@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:NP636110.RAMw8ch0ChLFA8DYn7Zde6nICGffQCQi8-9o8RwrpBFTU130_head { this: np:hasAssertion dgn-np:NP636110.RAMw8ch0ChLFA8DYn7Zde6nICGffQCQi8-9o8RwrpBFTU130_assertion; np:hasProvenance dgn-np:NP636110.RAMw8ch0ChLFA8DYn7Zde6nICGffQCQi8-9o8RwrpBFTU130_provenance; np:hasPublicationInfo dgn-np:NP636110.RAMw8ch0ChLFA8DYn7Zde6nICGffQCQi8-9o8RwrpBFTU130_publicationInfo; a np:Nanopublication . dgn-np:NP636110.RAMw8ch0ChLFA8DYn7Zde6nICGffQCQi8-9o8RwrpBFTU130_assertion a np:Assertion . dgn-np:NP636110.RAMw8ch0ChLFA8DYn7Zde6nICGffQCQi8-9o8RwrpBFTU130_provenance a np:Provenance . dgn-np:NP636110.RAMw8ch0ChLFA8DYn7Zde6nICGffQCQi8-9o8RwrpBFTU130_publicationInfo a np:PublicationInfo . } dgn-np:NP636110.RAMw8ch0ChLFA8DYn7Zde6nICGffQCQi8-9o8RwrpBFTU130_assertion { miriam-gene:675 a ncit:C16612 . lld:C0678222 a ncit:C7057 . dgn-gda:DGN5a170506e1f554b7cea10b58114ebdc8 sio:SIO_000628 miriam-gene:675, lld:C0678222; a sio:SIO_001121 . } dgn-np:NP636110.RAMw8ch0ChLFA8DYn7Zde6nICGffQCQi8-9o8RwrpBFTU130_provenance { dgn-np:NP636110.RAMw8ch0ChLFA8DYn7Zde6nICGffQCQi8-9o8RwrpBFTU130_assertion dcterms:description "[Our study shows that -26 5' UTR polymorphism in BRCA2 can modulate the fine-tuned regulation of the multifunctional gene BRCA2 and renders risk or protection according to the genotype status in the sporadic form of breast cancer, which is further influenced by the germline genetic backgrounds of codon 72 polymorphism of p53.]. 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:17945002; 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:NP636110.RAMw8ch0ChLFA8DYn7Zde6nICGffQCQi8-9o8RwrpBFTU130_publicationInfo { this: dcterms:created "2016-05-13T12:46:33+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" . }