Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1398651.RAmMbJ8FmoqM0Wd-Pop78OV6QhNwv_WKMH3iBcxkmZMWs130_assertion> ?p ?o ?g. }
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- NP1398651.RAmMbJ8FmoqM0Wd-Pop78OV6QhNwv_WKMH3iBcxkmZMWs130_assertion type Assertion NP1398651.RAmMbJ8FmoqM0Wd-Pop78OV6QhNwv_WKMH3iBcxkmZMWs130_head.
- NP1398651.RAmMbJ8FmoqM0Wd-Pop78OV6QhNwv_WKMH3iBcxkmZMWs130_assertion description "[Mutations in the gene encoding the homeobox transcription factor NKX2-5 were found to cause nonsyndromic, human congenital heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1398651.RAmMbJ8FmoqM0Wd-Pop78OV6QhNwv_WKMH3iBcxkmZMWs130_provenance.
- NP1398651.RAmMbJ8FmoqM0Wd-Pop78OV6QhNwv_WKMH3iBcxkmZMWs130_assertion evidence source_evidence_literature NP1398651.RAmMbJ8FmoqM0Wd-Pop78OV6QhNwv_WKMH3iBcxkmZMWs130_provenance.
- NP1398651.RAmMbJ8FmoqM0Wd-Pop78OV6QhNwv_WKMH3iBcxkmZMWs130_assertion SIO_000772 9651244 NP1398651.RAmMbJ8FmoqM0Wd-Pop78OV6QhNwv_WKMH3iBcxkmZMWs130_provenance.
- NP1398651.RAmMbJ8FmoqM0Wd-Pop78OV6QhNwv_WKMH3iBcxkmZMWs130_assertion wasDerivedFrom befree-2016 NP1398651.RAmMbJ8FmoqM0Wd-Pop78OV6QhNwv_WKMH3iBcxkmZMWs130_provenance.
- NP1398651.RAmMbJ8FmoqM0Wd-Pop78OV6QhNwv_WKMH3iBcxkmZMWs130_assertion wasGeneratedBy ECO_0000203 NP1398651.RAmMbJ8FmoqM0Wd-Pop78OV6QhNwv_WKMH3iBcxkmZMWs130_provenance.