Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_provenance.
- NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_provenance.
- NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_assertion evidence source_evidence_literature NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_provenance.
- NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_assertion SIO_000772 19412328 NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_provenance.
- NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_assertion wasDerivedFrom gad-20150221 NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_provenance.
- NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_assertion wasGeneratedBy ECO_0000203 NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_provenance.