Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_provenance.
- NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_assertion description "[Neither of the GST-null genotypes increased the risk for SCCA (p>0.05); however, the combination of the GSTM-1 and GSTT1-null genotypes showed a non-significant trend for an increased risk for developing cervical cancer with an adjusted OR of 2.7 (95%CI=0.8-9.0, p=0.10).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_provenance.
- NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_assertion evidence source_evidence_literature NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_provenance.
- NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_assertion SIO_000772 19640174 NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_provenance.
- NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_assertion wasDerivedFrom befree-2016 NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_provenance.
- NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_assertion wasGeneratedBy ECO_0000203 NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_provenance.
- befree-2016 importedOn "2016-02-19" NP754178.RAAGeHQ2uFAxy7Ykgbtj4ChGjA5MbNPZfk6xiOuCvm-h0130_provenance.