Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP151251.RArxqALDU33q6n2Jepn_LArs5esTGImB1q1uBXPwWxAgo130_provenance.