Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_provenance.
- NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_assertion description "[Detection of C677T mutation of MTHFR in subject with coronary heart disease by hairpin probe with enzymatic color on microarray.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_provenance.
- NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_assertion evidence source_evidence_literature NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_provenance.
- NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_assertion SIO_000772 21802936 NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_provenance.
- NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_assertion wasDerivedFrom befree-2016 NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_provenance.
- NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_assertion wasGeneratedBy ECO_0000203 NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_provenance.
- befree-2016 importedOn "2016-02-19" NP913553.RABFobNVOGLW0jJm-jzgqGQz7u7y8XEBOvXfqEvLEEcrs130_provenance.