Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_provenance.
- NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_assertion description "[High prevalence of somatic mutations in the cardiac transcription factor genes NKX2.5 and GATA4 have been reported in the affected cardiovascular tissue of patients with isolated cardiac septal defects, suggesting a role of somatic mutations in the pathogenesis of these congenital heart defects (CHDs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_provenance.
- NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_assertion evidence source_evidence_literature NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_provenance.
- NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_assertion SIO_000772 21276881 NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_provenance.
- NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_assertion wasDerivedFrom befree-20150227 NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_provenance.
- NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_assertion wasGeneratedBy ECO_0000203 NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP334022.RA5RqDz5fjEOlaR1ZPY3I5G7TQNwkp5ioKkMPsUjV_1mo130_provenance.