@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP839978.RAn9CKLDv_797KEcUyrwzbjH8ECUyDps_HooKEDa4Xht8130_head { this: np:hasAssertion dgn-np:NP839978.RAn9CKLDv_797KEcUyrwzbjH8ECUyDps_HooKEDa4Xht8130_assertion; np:hasProvenance dgn-np:NP839978.RAn9CKLDv_797KEcUyrwzbjH8ECUyDps_HooKEDa4Xht8130_provenance; np:hasPublicationInfo dgn-np:NP839978.RAn9CKLDv_797KEcUyrwzbjH8ECUyDps_HooKEDa4Xht8130_publicationInfo; a np:Nanopublication . dgn-np:NP839978.RAn9CKLDv_797KEcUyrwzbjH8ECUyDps_HooKEDa4Xht8130_assertion a np:Assertion . dgn-np:NP839978.RAn9CKLDv_797KEcUyrwzbjH8ECUyDps_HooKEDa4Xht8130_provenance a np:Provenance . dgn-np:NP839978.RAn9CKLDv_797KEcUyrwzbjH8ECUyDps_HooKEDa4Xht8130_publicationInfo a np:PublicationInfo . } dgn-np:NP839978.RAn9CKLDv_797KEcUyrwzbjH8ECUyDps_HooKEDa4Xht8130_assertion { miriam-gene:675 a ncit:C16612 . lld:C0476089 a ncit:C7057 . dgn-gda:DGN806d8765b2f84aaa8f51a1515232983e sio:SIO_000628 miriam-gene:675, lld:C0476089; a sio:SIO_001122 . } dgn-np:NP839978.RAn9CKLDv_797KEcUyrwzbjH8ECUyDps_HooKEDa4Xht8130_provenance { dgn-np:NP839978.RAn9CKLDv_797KEcUyrwzbjH8ECUyDps_HooKEDa4Xht8130_assertion dcterms:description "[Unselected Jewish women with EC who were diagnosed from January 1982 to January 2008 were genotyped for the predominant mutations in Jewish individuals in BRCA1 (185delAG, 5382InsC, Tyr978X) BRCA2 (6174delT), MSH2 (A636P, 324delCA) and MSH6 (c.3984_3987dup).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:20850175; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP839978.RAn9CKLDv_797KEcUyrwzbjH8ECUyDps_HooKEDa4Xht8130_publicationInfo { this: dcterms:created "2016-05-13T12:48:05+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }