@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:NP553557.RAOqnlShKf-oVkhbkcAkada1Px11q1f_fEQlPP_WrFwJM130_head { this: np:hasAssertion dgn-np:NP553557.RAOqnlShKf-oVkhbkcAkada1Px11q1f_fEQlPP_WrFwJM130_assertion; np:hasProvenance dgn-np:NP553557.RAOqnlShKf-oVkhbkcAkada1Px11q1f_fEQlPP_WrFwJM130_provenance; np:hasPublicationInfo dgn-np:NP553557.RAOqnlShKf-oVkhbkcAkada1Px11q1f_fEQlPP_WrFwJM130_publicationInfo; a np:Nanopublication . dgn-np:NP553557.RAOqnlShKf-oVkhbkcAkada1Px11q1f_fEQlPP_WrFwJM130_assertion a np:Assertion . dgn-np:NP553557.RAOqnlShKf-oVkhbkcAkada1Px11q1f_fEQlPP_WrFwJM130_provenance a np:Provenance . dgn-np:NP553557.RAOqnlShKf-oVkhbkcAkada1Px11q1f_fEQlPP_WrFwJM130_publicationInfo a np:PublicationInfo . } dgn-np:NP553557.RAOqnlShKf-oVkhbkcAkada1Px11q1f_fEQlPP_WrFwJM130_assertion { miriam-gene:672 a ncit:C16612 . lld:C0029925 a ncit:C7057 . dgn-gda:DGN85547b434d0fc39615a07ff1e470eb30 sio:SIO_000628 miriam-gene:672, lld:C0029925; a sio:SIO_001121 . } dgn-np:NP553557.RAOqnlShKf-oVkhbkcAkada1Px11q1f_fEQlPP_WrFwJM130_provenance { dgn-np:NP553557.RAOqnlShKf-oVkhbkcAkada1Px11q1f_fEQlPP_WrFwJM130_assertion dcterms:description "[A total of 104 patients with breast and/or ovarian cancer whose genetic counselling answered the criteria of the American Society of Clinical Oncology (ASCO 2003), were prospectively screened for mutations in all coding exons of the BRCA1 gene by automatic direct sequencing.]. 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:16760288; 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:NP553557.RAOqnlShKf-oVkhbkcAkada1Px11q1f_fEQlPP_WrFwJM130_publicationInfo { this: dcterms:created "2016-05-13T12:45:55+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" . }