Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_provenance.
- NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_assertion description "[In a hospital-based study of 805 non-Hispanic white patients with CM and 835 cancer-free age-, sex-, and ethnicity-matched controls, we genotyped three reported putatively functional polymorphisms of CASP8 and CASP10-CASP8 D302 H (rs1045485:G>C), CASP8 -652 6N del (rs3834129:-/CTTACT), and CASP10 I522L (rs13006529:A>T)-and assessed their associations with risk of CM and interactions with known risk factors for CM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_provenance.
- NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_assertion evidence source_evidence_literature NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_provenance.
- NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_assertion SIO_000772 18563783 NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_provenance.
- NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_assertion wasDerivedFrom befree-20140225 NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_provenance.
- NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_assertion wasGeneratedBy ECO_0000203 NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP392582.RA6OMsBW8NNBtuGPZL7lNIKWWHN1Y9fk7Mi8KbbNlsUXw130_provenance.