Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_provenance.
- NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_assertion wasGeneratedBy ECO_0000203 NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_provenance.
- NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_assertion wasDerivedFrom befree-20150227 NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_provenance.
- NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_assertion SIO_000772 21091212 NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_provenance.
- NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_assertion evidence source_evidence_literature NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_provenance.
- NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_assertion description "[The sixth SNP 1212G>T in the 3'UTR was observed in 40% of the CHD cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791518.RAAssG8NAB7W0Ro-w4vf0E83iwSWTisGd0d-h5jBGBdNk130_provenance.