Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_provenance.
- NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_assertion description "[No associations were found between IL1B C(-31)T or IL1RN VNTR genotypes, alleles or haplotypes and the severity of CAD when subgroups with SVD and MVD were compared.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_provenance.
- NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_assertion evidence source_evidence_literature NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_provenance.
- NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_assertion SIO_000772 21840356 NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_provenance.
- NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_assertion wasDerivedFrom befree-20150227 NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_provenance.
- NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_assertion wasGeneratedBy ECO_0000203 NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_provenance.