Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_provenance.
- NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_assertion description "[The predominant cardiac defects in Fgfr2-IIIb mutant embryos are ventricular septal defects associated with overriding aorta or double outlet right ventricle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_provenance.
- NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_assertion evidence source_evidence_literature NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_provenance.
- NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_assertion SIO_000772 16687131 NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_provenance.
- NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_assertion wasDerivedFrom befree-2016 NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_provenance.
- NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_assertion wasGeneratedBy ECO_0000203 NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_provenance.
- befree-2016 importedOn "2016-02-19" NP549084.RA36wO_KR6w9d0lJcpZhum3pomV_KAKsboLWLH-oTOoYk130_provenance.