Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_assertion> ?p ?o ?g. }
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- NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_assertion type Assertion NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_head.
- NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_assertion wasGeneratedBy ECO_0000203 NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_provenance.
- NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_assertion wasDerivedFrom lhgdn-20090331 NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_provenance.
- NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_assertion SIO_000772 12798584 NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_provenance.
- NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_assertion evidence source_evidence_literature NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_provenance.
- NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_assertion description "[NKX2-5 mutations are a relatively infrequent cause of sporadic ASD (atrial septal defect) and HLHS (hypoplastic left heart syndrome)/for NKX2-5 mutations warranted in individuals with ASD family history, irrespective of AV conduction block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP200061.RACWYa0dPooOHF-7s8hadX3aA9bbB_CakCmn1RTMx_IDU130_provenance.