Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_provenance.
- NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_assertion description "[Across RXRA, one haplotype located 3' of the coding sequence (rs748964, rs3118523), increased RCC risk 35% among individuals with the variant haplotype compared to those with the most common haplotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_provenance.
- NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_assertion evidence source_evidence_literature NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_provenance.
- NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_assertion SIO_000772 19753122 NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_provenance.
- NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_assertion wasDerivedFrom gad-20150221 NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_provenance.
- NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_assertion wasGeneratedBy ECO_0000203 NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP125792.RASd8mU986JYwn0FjffHndMxYnygsjGwJQljecbulMUbU130_provenance.