@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:NP1249865.RAODnPfej6-W7p_OJmVeMvAPgfI9QWWPV1BlhGFR-TQzI130_head { this: np:hasAssertion dgn-np:NP1249865.RAODnPfej6-W7p_OJmVeMvAPgfI9QWWPV1BlhGFR-TQzI130_assertion; np:hasProvenance dgn-np:NP1249865.RAODnPfej6-W7p_OJmVeMvAPgfI9QWWPV1BlhGFR-TQzI130_provenance; np:hasPublicationInfo dgn-np:NP1249865.RAODnPfej6-W7p_OJmVeMvAPgfI9QWWPV1BlhGFR-TQzI130_publicationInfo; a np:Nanopublication . dgn-np:NP1249865.RAODnPfej6-W7p_OJmVeMvAPgfI9QWWPV1BlhGFR-TQzI130_assertion a np:Assertion . dgn-np:NP1249865.RAODnPfej6-W7p_OJmVeMvAPgfI9QWWPV1BlhGFR-TQzI130_provenance a np:Provenance . dgn-np:NP1249865.RAODnPfej6-W7p_OJmVeMvAPgfI9QWWPV1BlhGFR-TQzI130_publicationInfo a np:PublicationInfo . } dgn-np:NP1249865.RAODnPfej6-W7p_OJmVeMvAPgfI9QWWPV1BlhGFR-TQzI130_assertion { miriam-gene:672 a ncit:C16612 . lld:C3539878 a ncit:C7057 . dgn-gda:DGNa6202efb5116e1f5455df1d6321dde7b sio:SIO_000628 miriam-gene:672, lld:C3539878; a sio:SIO_001121 . } dgn-np:NP1249865.RAODnPfej6-W7p_OJmVeMvAPgfI9QWWPV1BlhGFR-TQzI130_provenance { dgn-np:NP1249865.RAODnPfej6-W7p_OJmVeMvAPgfI9QWWPV1BlhGFR-TQzI130_assertion dcterms:description "[These tumors account for 12-17 % of all breast cancers, preferentially affect young women, are more frequent in women of African and Hispanic descent, and are enriched in the population of patients diagnosed with interval cancers. TNBCs account for the majority of breast cancers arising in BRCA1 germline mutation carriers (approximately 80%), and approximately 11-16% of all TNBCs harbor BRCA1 or BRCA2 germline mutations.]. 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:25527230; 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:NP1249865.RAODnPfej6-W7p_OJmVeMvAPgfI9QWWPV1BlhGFR-TQzI130_publicationInfo { this: dcterms:created "2016-05-13T12:51:12+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" . }