@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:NP663859.RAQ8jtcjs4T5ERtAmBPbqqt38mFNA__T95pvJwad_qtfQ130_head { this: np:hasAssertion dgn-np:NP663859.RAQ8jtcjs4T5ERtAmBPbqqt38mFNA__T95pvJwad_qtfQ130_assertion; np:hasProvenance dgn-np:NP663859.RAQ8jtcjs4T5ERtAmBPbqqt38mFNA__T95pvJwad_qtfQ130_provenance; np:hasPublicationInfo dgn-np:NP663859.RAQ8jtcjs4T5ERtAmBPbqqt38mFNA__T95pvJwad_qtfQ130_publicationInfo; a np:Nanopublication . dgn-np:NP663859.RAQ8jtcjs4T5ERtAmBPbqqt38mFNA__T95pvJwad_qtfQ130_assertion a np:Assertion . dgn-np:NP663859.RAQ8jtcjs4T5ERtAmBPbqqt38mFNA__T95pvJwad_qtfQ130_provenance a np:Provenance . dgn-np:NP663859.RAQ8jtcjs4T5ERtAmBPbqqt38mFNA__T95pvJwad_qtfQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP663859.RAQ8jtcjs4T5ERtAmBPbqqt38mFNA__T95pvJwad_qtfQ130_assertion { miriam-gene:5889 a ncit:C16612 . lld:C0346153 a ncit:C7057 . dgn-gda:DGN2a4b600bd523da05d174b4af1a306571 sio:SIO_000628 miriam-gene:5889, lld:C0346153; a sio:SIO_001122 . } dgn-np:NP663859.RAQ8jtcjs4T5ERtAmBPbqqt38mFNA__T95pvJwad_qtfQ130_provenance { dgn-np:NP663859.RAQ8jtcjs4T5ERtAmBPbqqt38mFNA__T95pvJwad_qtfQ130_assertion dcterms:description "[RAD51C c.-13_14del27 was observed in one familial breast cancer case and c.774delT in one unselected ovarian cancer case, thus confirming that RAD51C mutations are implicated in breast and ovarian cancer predisposition, although their overall frequency seems to be low.]. 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:21750962; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP663859.RAQ8jtcjs4T5ERtAmBPbqqt38mFNA__T95pvJwad_qtfQ130_publicationInfo { this: dcterms:created "2015-08-25T14:44:19+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }