Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_provenance.
- NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_assertion wasGeneratedBy ECO_0000203 NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_provenance.
- NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_assertion wasDerivedFrom befree-20150227 NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_provenance.
- NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_assertion SIO_000772 17611253 NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_provenance.
- NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_assertion evidence source_evidence_literature NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_provenance.
- NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_assertion description "[Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221849.RAHY46rAjZ9P2xiZoBwGc3jRphW_EoyxJIgFiGTDp_eOo130_provenance.