@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:NP550005.RAkz0lb9LzCi5qpu238Phwus_uriN3802NvRrmjcC8VnA130_head { this: np:hasAssertion dgn-np:NP550005.RAkz0lb9LzCi5qpu238Phwus_uriN3802NvRrmjcC8VnA130_assertion; np:hasProvenance dgn-np:NP550005.RAkz0lb9LzCi5qpu238Phwus_uriN3802NvRrmjcC8VnA130_provenance; np:hasPublicationInfo dgn-np:NP550005.RAkz0lb9LzCi5qpu238Phwus_uriN3802NvRrmjcC8VnA130_publicationInfo; a np:Nanopublication . dgn-np:NP550005.RAkz0lb9LzCi5qpu238Phwus_uriN3802NvRrmjcC8VnA130_assertion a np:Assertion . dgn-np:NP550005.RAkz0lb9LzCi5qpu238Phwus_uriN3802NvRrmjcC8VnA130_provenance a np:Provenance . dgn-np:NP550005.RAkz0lb9LzCi5qpu238Phwus_uriN3802NvRrmjcC8VnA130_publicationInfo a np:PublicationInfo . } dgn-np:NP550005.RAkz0lb9LzCi5qpu238Phwus_uriN3802NvRrmjcC8VnA130_assertion { miriam-gene:672 a ncit:C16612 . lld:C0346153 a ncit:C7057 . dgn-gda:DGN763f654ee36ba37285ee8fc6ad936263 sio:SIO_000628 miriam-gene:672, lld:C0346153; a sio:SIO_001122 . } dgn-np:NP550005.RAkz0lb9LzCi5qpu238Phwus_uriN3802NvRrmjcC8VnA130_provenance { dgn-np:NP550005.RAkz0lb9LzCi5qpu238Phwus_uriN3802NvRrmjcC8VnA130_assertion dcterms:description "[The analysis of 816 BRCA1/2 mutation-negative familial breast cancer patients and 1012 controls revealed an association of the PPARGC1A Thr612Met polymorphism with familial breast cancer (OR = 1.35, 95% CI 1.00-1.81, P = 0.049), high-risk familial breast cancer (OR = 1.51, 95% CI 1.08-2.12, P = 0.017) and bilateral familial breast cancer (OR = 2.30, 95% CI 1.24-4.28, P = 0.009).]. 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:16704985; 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:NP550005.RAkz0lb9LzCi5qpu238Phwus_uriN3802NvRrmjcC8VnA130_publicationInfo { this: dcterms:created "2016-05-13T12:45:54+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" . }