As of 2022-03-07, the Wikidata property PubMed Health (P653) is used on 7 items as main value on statements (not counting qualifiers) of the Q and P namespaces.

Closest properties: by cardinality of intersection, by Jaccard index.

Display properties of the following types:                                    

Closest properties by cardinality of intersection

IDLabelIntersection cardinalityJaccard index
P780 symptoms and signs 7
 0.0040
P604 MedlinePlus ID 7
 0.0035
P673 eMedicine ID 7
 0.0027
P557 DiseasesDB 7
 0.0023
P1995 health specialty 7
 0.0008
P8408 KBpedia ID 7
 0.0002
P1417 Encyclopædia Britannica Online ID 7
 0.0000
P5008 on focus list of Wikimedia project 7
 0.0000
P279 subclass of 7
 0.0000
P373 Commons category 7
 0.0000
P18 image 7
 0.0000
P646 Freebase ID 7
 0.0000
P31 instance of 7
 0.0000
P1461 Patientplus ID 6
 0.0079
P5082 Store medisinske leksikon ID 6
 0.0020
P7329 ID (MMS) 6
 0.0008
P4229 ICD-10-CM 6
 0.0007
P7807 ICD-11 (foundation) 6
 0.0006
P699 Disease Ontology ID 6
 0.0006
P665 KEGG ID 6
 0.0003
P2347 YSO ID 6
 0.0003
P2892 UMLS CUI 6
 0.0002
P3827 JSTOR topic ID 6
 0.0002
P10283 OpenAlex ID 6
 0.0001
P910 topic's main category 6
 0.0000
P2888 exact match 6
 0.0000
P667 ICPC 2 ID 5
 0.0053
P2176 drug or therapy used for treatment 5
 0.0038
P3471 WikiSkripta ID 5
 0.0021
P1692 ICD-9-CM 5
 0.0012
P1748 NCI Thesaurus ID 5
 0.0005
P672 MeSH tree code 5
 0.0003
P492 OMIM ID 5
 0.0002
P486 MeSH descriptor ID 5
 0.0001
P349 National Diet Library ID 5
 0.0000
P8189 National Library of Israel J9U ID 5
 0.0000
P3417 Quora topic ID 5
 0.0000
P227 GND ID 5
 0.0000
P244 Library of Congress authority ID 5
 0.0000
P923 medical examinations 4
 0.0120
P7995 NHS Health A to Z ID 4
 0.0074
P493 ICD-9 4
 0.0010
P494 ICD-10 4
 0.0009
P2293 genetic association 4
 0.0005
P6366 Microsoft Academic ID 4
 0.0000
P5642 risk factor 3
 0.0246
P7464 Genetics Home Reference Conditions ID 3
 0.0039
P3841 Human Phenotype Ontology ID 3
 0.0017
P4317 GARD rare disease ID 3
 0.0006
P828 has cause 3
 0.0004

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P1395 National Cancer Institute ID 1
 0.0455
P1583 MalaCards ID 2
 0.0400
P5642 risk factor 3
 0.0246
P2074 internetmedicin.se ID 1
 0.0149
P3292 DocCheck Flexikon De ID 1
 0.0130
P923 medical examinations 4
 0.0120
P1199 mode of inheritance 1
 0.0111
P1193 prevalence 1
 0.0106
P6532 has phenotype 1
 0.0095
P3487 maximal incubation period in humans 1
 0.0083
P3488 minimal incubation period in humans 1
 0.0082
P1461 Patientplus ID 6
 0.0079
P1605 has natural reservoir 1
 0.0078
P7995 NHS Health A to Z ID 4
 0.0074
P668 GeneReviews ID 1
 0.0064
P667 ICPC 2 ID 5
 0.0053
P1060 pathogen transmission process 1
 0.0048
P780 symptoms and signs 7
 0.0040
P7464 Genetics Home Reference Conditions ID 3
 0.0039
P2176 drug or therapy used for treatment 5
 0.0038
P604 MedlinePlus ID 7
 0.0035
P924 possible treatment 1
 0.0032
P673 eMedicine ID 7
 0.0027
P557 DiseasesDB 7
 0.0023
P3471 WikiSkripta ID 5
 0.0021
P5082 Store medisinske leksikon ID 6
 0.0020
P9084 ABC News topic ID 2
 0.0019
P3841 Human Phenotype Ontology ID 3
 0.0017
P1692 ICD-9-CM 5
 0.0012
P493 ICD-9 4
 0.0010
P494 ICD-10 4
 0.0009
P9287 Cyprus Bibliography ID 1
 0.0009
P1995 health specialty 7
 0.0008
P6293 YSA ID 2
 0.0008
P6200 BBC News topic ID 1
 0.0008
P3885 History of Modern Biomedicine ID 1
 0.0008
P7329 ID (MMS) 6
 0.0008
P689 afflicts 1
 0.0008
P4229 ICD-10-CM 6
 0.0007
P4317 GARD rare disease ID 3
 0.0006
P7807 ICD-11 (foundation) 6
 0.0006
P699 Disease Ontology ID 6
 0.0006
P1748 NCI Thesaurus ID 5
 0.0005
P2293 genetic association 4
 0.0005
P8309 Yle topic ID 2
 0.0005
P1542 has effect 2
 0.0005
P828 has cause 3
 0.0004
P3569 Cultureel Woordenboek ID 2
 0.0004
P6573 Klexikon article ID 1
 0.0004
P927 anatomical location 1
 0.0004