@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:NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_head { this: np:hasAssertion dgn-np:NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_assertion; np:hasProvenance dgn-np:NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_provenance; np:hasPublicationInfo dgn-np:NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_publicationInfo; a np:Nanopublication . dgn-np:NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_assertion a np:Assertion . dgn-np:NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_provenance a np:Provenance . dgn-np:NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_publicationInfo a np:PublicationInfo . } dgn-np:NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_assertion { miriam-gene:675 a ncit:C16612 . lld:C1333600 a ncit:C7057 . dgn-gda:DGN052207827a52e9b717308a3eb3daca19 sio:SIO_000628 miriam-gene:675, lld:C1333600; a sio:SIO_001121 . } dgn-np:NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_provenance { dgn-np:NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_assertion dcterms:description "[This review article will discuss (1) the BRCA1 and BRCA2 genes within the larger context of homologous recombination deficiency; (2) the advances in our understanding of hereditary cancer risk and the dramatic shifts that have occurred in the genetic testing landscape since the landmark 2013 Supreme Court ruling invalidating patents on BRCA1 and BRCA2 genetic testing; and (3) the clinical trials leading to the approval of olaparib, the first in human PARP inhibitor.]. 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:25725131; 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:NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_publicationInfo { this: dcterms:created "2016-05-13T12:51:20+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" . }