Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_provenance.
- NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_assertion description "[To test the hypothesis that actin dysfunction leads to heart failure, patients with hereditary idiopathic dilated cardiomyopathy (IDC) were examined for mutations in the cardiac actin gene (ACTC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_provenance.
- NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_assertion evidence source_evidence_literature NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_provenance.
- NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_assertion SIO_000772 9563954 NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_provenance.
- NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_assertion wasDerivedFrom befree-20140225 NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_provenance.
- NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_assertion wasGeneratedBy ECO_0000203 NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_provenance.
- befree-20140225 importedOn "2014-02-25" NP483237.RAeI06Onoo2K6sM5-opNsMUucVW3rHdZfJgIEldIOb-84130_provenance.