Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_provenance.
- NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_assertion wasGeneratedBy ECO_0000203 NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_provenance.
- NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_assertion wasDerivedFrom befree-2016 NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_provenance.
- NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_assertion SIO_000772 24519899 NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_provenance.
- NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_assertion evidence source_evidence_literature NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_provenance.
- NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_assertion description "[However, cases carrying haplotypes with variant alleles of both CYP1A1*2A and *2C or CYP1B1*2 and *3 or CYP2E1*5B and *6 were at significant risk of developing HNSCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1154418.RAE1FMdJMhs1H0SzA497mv_VJFvbfpnbUDIa7v56pVVX4130_provenance.