Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_provenance.
- NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_assertion description "[Our results suggest a modestly increased risk for SPM after index SCCHN with FAS -670 A > G and FASLG -844 C > T polymorphisms and an even greater risk for SPM with multiple combined FAS and FASLG risk genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_provenance.
- NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_assertion evidence source_evidence_literature NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_provenance.
- NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_assertion SIO_000772 20501759 NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_provenance.
- NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_assertion wasDerivedFrom befree-20140225 NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_provenance.
- NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_assertion wasGeneratedBy ECO_0000203 NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP507196.RAsTH8KKrTWMXwYuKuerkZ__TLZBybvWLRiZ08MvHXroE130_provenance.