Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_provenance.
- NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_assertion description "[A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_provenance.
- NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_assertion evidence source_evidence_literature NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_provenance.
- NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_assertion SIO_000772 25503402 NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_provenance.
- NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_assertion wasDerivedFrom befree-2016 NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_provenance.
- NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_assertion wasGeneratedBy ECO_0000203 NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_provenance.
- befree-2016 importedOn "2016-02-19" NP1247898.RAR11FvfQWbhb4YC3yMJJ3hY5axIUlTGzY4osJp0H6o4w130_provenance.