@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:NP263837.RABIXTLwpZydhw_QMUNlZxXEWL19tTl_s_FUUHNx8IJfY130_head { this: np:hasAssertion dgn-np:NP263837.RABIXTLwpZydhw_QMUNlZxXEWL19tTl_s_FUUHNx8IJfY130_assertion; np:hasProvenance dgn-np:NP263837.RABIXTLwpZydhw_QMUNlZxXEWL19tTl_s_FUUHNx8IJfY130_provenance; np:hasPublicationInfo dgn-np:NP263837.RABIXTLwpZydhw_QMUNlZxXEWL19tTl_s_FUUHNx8IJfY130_publicationInfo; a np:Nanopublication . dgn-np:NP263837.RABIXTLwpZydhw_QMUNlZxXEWL19tTl_s_FUUHNx8IJfY130_assertion a np:Assertion . dgn-np:NP263837.RABIXTLwpZydhw_QMUNlZxXEWL19tTl_s_FUUHNx8IJfY130_provenance a np:Provenance . dgn-np:NP263837.RABIXTLwpZydhw_QMUNlZxXEWL19tTl_s_FUUHNx8IJfY130_publicationInfo a np:PublicationInfo . } dgn-np:NP263837.RABIXTLwpZydhw_QMUNlZxXEWL19tTl_s_FUUHNx8IJfY130_assertion { miriam-gene:672 a ncit:C16612 . lld:C0033578 a ncit:C7057 . dgn-gda:DGN735aa816ac9d5bca4887ae96de3c5c97 sio:SIO_000628 miriam-gene:672, lld:C0033578; a sio:SIO_001121 . } dgn-np:NP263837.RABIXTLwpZydhw_QMUNlZxXEWL19tTl_s_FUUHNx8IJfY130_provenance { dgn-np:NP263837.RABIXTLwpZydhw_QMUNlZxXEWL19tTl_s_FUUHNx8IJfY130_assertion dcterms:description "[PSA testing, six-core biopsy, genetic counselling and mutation analysis for French Canadian founder mutations in the BRCA1 and BRCA2 genes, histopathological review of tumour tissue from family members, examination of loss of heterozygosity at the BRCA2 gene locus, immunohistochemistry to determine the expression of the ERG nuclear oncoprotein in prostate tumours, genotyping with eight selected risk-associated single nucleotide polymorphisms, Doppler ultrasonography of the leg, CT of the abdomen and pelvis with intravenous and oral contrast, chest CT with intravenous contrast for the assessment of metastatic prostate cancer, genetic testing for the G84E variant in the HOXB13 gene.]. 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:23318356; 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:NP263837.RABIXTLwpZydhw_QMUNlZxXEWL19tTl_s_FUUHNx8IJfY130_publicationInfo { this: dcterms:created "2014-10-02T12:34:27+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" . }