Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_provenance.
- NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_assertion description "[Several mutations have been described for the transcription factor NKX2-5, and co-segregate with varied cardiac anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_provenance.
- NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_assertion evidence source_evidence_literature NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_provenance.
- NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_assertion SIO_000772 17184575 NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_provenance.
- NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_assertion wasDerivedFrom befree-2016 NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_provenance.
- NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_assertion wasGeneratedBy ECO_0000203 NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_provenance.
- befree-2016 importedOn "2016-02-19" NP585585.RAiPaibeet4ylgkKR5xTVm6mI4HNTdI9TS4z2PInOwH3o130_provenance.