@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:NP302657.RAy__I9GsAgQqAu6caa9EbbeEj_WBp6cZ0bCvUrJ1F3Uw130_head { this: np:hasAssertion dgn-np:NP302657.RAy__I9GsAgQqAu6caa9EbbeEj_WBp6cZ0bCvUrJ1F3Uw130_assertion; np:hasProvenance dgn-np:NP302657.RAy__I9GsAgQqAu6caa9EbbeEj_WBp6cZ0bCvUrJ1F3Uw130_provenance; np:hasPublicationInfo dgn-np:NP302657.RAy__I9GsAgQqAu6caa9EbbeEj_WBp6cZ0bCvUrJ1F3Uw130_publicationInfo; a np:Nanopublication . dgn-np:NP302657.RAy__I9GsAgQqAu6caa9EbbeEj_WBp6cZ0bCvUrJ1F3Uw130_assertion a np:Assertion . dgn-np:NP302657.RAy__I9GsAgQqAu6caa9EbbeEj_WBp6cZ0bCvUrJ1F3Uw130_provenance a np:Provenance . dgn-np:NP302657.RAy__I9GsAgQqAu6caa9EbbeEj_WBp6cZ0bCvUrJ1F3Uw130_publicationInfo a np:PublicationInfo . } dgn-np:NP302657.RAy__I9GsAgQqAu6caa9EbbeEj_WBp6cZ0bCvUrJ1F3Uw130_assertion { miriam-gene:672 a ncit:C16612 . lld:C0238122 a ncit:C7057 . dgn-gda:DGN428dc8762795665d01fb3515f2a940c4 sio:SIO_000628 miriam-gene:672, lld:C0238122; a sio:SIO_001121 . } dgn-np:NP302657.RAy__I9GsAgQqAu6caa9EbbeEj_WBp6cZ0bCvUrJ1F3Uw130_provenance { dgn-np:NP302657.RAy__I9GsAgQqAu6caa9EbbeEj_WBp6cZ0bCvUrJ1F3Uw130_assertion dcterms:description "[These findings support the recommendations that in this high-risk population (1) the fallopian tubes and ovaries should be submitted entirely and be evaluated by a pathologist with expertise in gynecologic malignancies in serial sections; (2) laparoscopy and laparotomy are the surgical modalities of choice to allow inspection of the peritoneal surfaces at time of prophylactic oophorectomy and collect fluid for cytologic evaluation; (3) despite the rarity of fallopian tube carcinoma in the general population, BRCA1 and BRCA2 mutation carriers may be at increased risk for tubal cancers.]. 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:12468342; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP302657.RAy__I9GsAgQqAu6caa9EbbeEj_WBp6cZ0bCvUrJ1F3Uw130_publicationInfo { this: dcterms:created "2014-10-02T12:34:54+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }