Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_assertion> ?p ?o ?g. }
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- NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_assertion type Assertion NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_head.
- NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_assertion wasGeneratedBy ECO_0000203 NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance.
- NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_assertion wasDerivedFrom gad-20150221 NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance.
- NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_assertion SIO_000772 12798584 NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance.
- NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_assertion evidence source_evidence_literature NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance.
- NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_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." NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance.