Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_provenance.
- NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_assertion description "[The TYR haplotype carrying only the Arg402Gln variant allele was significantly associated with SCC risk (OR, 1.35; 95% CI, 1.04-1.74).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_provenance.
- NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_assertion evidence source_evidence_literature NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_provenance.
- NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_assertion SIO_000772 19384953 NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_provenance.
- NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_assertion wasDerivedFrom gad-20150221 NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_provenance.
- NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_assertion wasGeneratedBy ECO_0000203 NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_provenance.
- gad-20150221 importedOn "2015-02-21" NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_provenance.