Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_provenance.
- NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_assertion wasGeneratedBy ECO_0000203 NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_provenance.
- NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_assertion wasDerivedFrom befree-20150227 NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_provenance.
- NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_assertion SIO_000772 10587520 NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_provenance.
- NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_assertion evidence source_evidence_literature NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_provenance.
- NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_assertion description "[Mutations in human NKX2.5 cause a variety of cardiac anomalies and may account for a clinically significant portion of tetralogy of Fallot and idiopathic AV block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333974.RAqhDY21m6Vj1tU5qZ05kqXFtjaVxeyBHd1W7oEzhAMS4130_provenance.