Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_assertion type Assertion NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_head.
- NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_assertion wasGeneratedBy ECO_0000203 NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_provenance.
- NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_assertion wasDerivedFrom lhgdn-20090331 NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_provenance.
- NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_assertion SIO_000772 12798584 NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_provenance.
- NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_assertion evidence source_evidence_literature NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_provenance.
- NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_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." NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_provenance.