@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:NP354051.RA0vQeyrpD9h4N_j2k8EMAc9B7ogWdyuVA3nxzR63sunc130_head { this: np:hasAssertion dgn-np:NP354051.RA0vQeyrpD9h4N_j2k8EMAc9B7ogWdyuVA3nxzR63sunc130_assertion; np:hasProvenance dgn-np:NP354051.RA0vQeyrpD9h4N_j2k8EMAc9B7ogWdyuVA3nxzR63sunc130_provenance; np:hasPublicationInfo dgn-np:NP354051.RA0vQeyrpD9h4N_j2k8EMAc9B7ogWdyuVA3nxzR63sunc130_publicationInfo; a np:Nanopublication . dgn-np:NP354051.RA0vQeyrpD9h4N_j2k8EMAc9B7ogWdyuVA3nxzR63sunc130_assertion a np:Assertion . dgn-np:NP354051.RA0vQeyrpD9h4N_j2k8EMAc9B7ogWdyuVA3nxzR63sunc130_provenance a np:Provenance . dgn-np:NP354051.RA0vQeyrpD9h4N_j2k8EMAc9B7ogWdyuVA3nxzR63sunc130_publicationInfo a np:PublicationInfo . } dgn-np:NP354051.RA0vQeyrpD9h4N_j2k8EMAc9B7ogWdyuVA3nxzR63sunc130_assertion { miriam-gene:1728 a ncit:C16612 . lld:C0178874 a ncit:C7057 . dgn-gda:DGN03b87a0e28516422d8d94936f52faec0 sio:SIO_000628 miriam-gene:1728, lld:C0178874; a sio:SIO_001122 . } dgn-np:NP354051.RA0vQeyrpD9h4N_j2k8EMAc9B7ogWdyuVA3nxzR63sunc130_provenance { dgn-np:NP354051.RA0vQeyrpD9h4N_j2k8EMAc9B7ogWdyuVA3nxzR63sunc130_assertion dcterms:description "[Our data showed that (1) the frequency of C609T NQO1 was significantly increased in TNM stage III HCC patients; (2) no significant association was found between p53 expression and C609T polymorphism of NQO1 gene; and (3) a tumor/non-tumor (T/N) ratio > 1.27 of NQO1 expression revealed by real-time qPCR analyses was positively correlated with poorer survival in patients with tumors >5 cm, suggesting that an increase of NQO1 expression may be an indicator of advanced tumor progression.]. 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:19688691; 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:NP354051.RA0vQeyrpD9h4N_j2k8EMAc9B7ogWdyuVA3nxzR63sunc130_publicationInfo { this: dcterms:created "2015-08-25T14:41:04+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" . }