Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_assertion> ?p ?o ?g. }
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- NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_assertion type Assertion NP580284.RAHmGNoEmPxqh4SY28Jxp2gSoAwUo5LATeMgMTe9CJqDc130_head.
- 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.