Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_provenance.
- NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_assertion description "[Further quantification of the extent of CVD risk conferred by UGT1A gene family variants in a high risk cohort with T2D is still required.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_provenance.
- NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_assertion evidence source_evidence_literature NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_provenance.
- NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_assertion SIO_000772 23642732 NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_provenance.
- NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_assertion wasDerivedFrom befree-20150227 NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_provenance.
- NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_assertion wasGeneratedBy ECO_0000203 NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_provenance.
- befree-20150227 importedOn "2015-02-27" NP766256.RAduTRMOwIzO2pUwgSZlcNJhupxGuHfIKWBqLt1lAfqec130_provenance.