Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_provenance.
- NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_assertion description "[NKX2.5 mutations occur in a small percentage of patients with various CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_provenance.
- NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_assertion evidence source_evidence_literature NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_provenance.
- NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_assertion SIO_000772 14607454 NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_provenance.
- NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_assertion wasDerivedFrom befree-2016 NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_provenance.
- NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_assertion wasGeneratedBy ECO_0000203 NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_provenance.
- befree-2016 importedOn "2016-02-19" NP419884.RA9KlH-wnmSI-DWFaSV54HuEg0KRgf_9xcMxpv5VFZDbY130_provenance.