Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_provenance.
- NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_assertion description "[The combined results indicate, for the first time, that ACTC1 mutations or reduced ACTC1 levels may lead to ASD without signs of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_provenance.
- NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_assertion evidence source_evidence_literature NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_provenance.
- NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_assertion SIO_000772 17947298 NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_provenance.
- NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_assertion wasDerivedFrom befree-20150227 NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_provenance.
- NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_assertion wasGeneratedBy ECO_0000203 NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP221868.RA4zmxDLqyI2rY5OWN17RB-yoIMspSJpjqmaHgdrlqIvw130_provenance.