Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance.
- befree-2016 importedOn "2016-02-19" NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance.
- NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_assertion wasGeneratedBy ECO_0000203 NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance.
- NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_assertion wasDerivedFrom befree-2016 NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance.
- NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_assertion SIO_000772 12798584 NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance.
- NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_assertion evidence source_evidence_literature NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance.
- NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_assertion description "[Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397685.RALC1bl1b_axu9fbZhqCkFK8IsqhEfA3d1oEUGwSLY7Cs130_provenance.