Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_provenance.
- NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_assertion description "[The effects of S185F are compared with those of two mutations in residues 175 and 180 of human alpha-tropomyosin 1 which cause familial hypertrophic cardiomyopathy (HCM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_provenance.
- NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_assertion evidence source_evidence_literature NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_provenance.
- NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_assertion SIO_000772 11359941 NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_provenance.
- NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_assertion wasDerivedFrom befree-2016 NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_provenance.
- NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_assertion wasGeneratedBy ECO_0000203 NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_provenance.
- befree-2016 importedOn "2016-02-19" NP318471.RABsIIOTmLu_VgnIX80a3i0CKVf-IHBho680iZIFAy7cs130_provenance.