Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_provenance.
- NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_assertion description "[identification of a missense mutation of the AVP-NPII gene and a novel mutation predicting a truncated protein in the gene in familial central diabetes insipidus]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_provenance.
- NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_assertion evidence source_evidence_literature NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_provenance.
- NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_assertion SIO_000772 12012274 NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_provenance.
- NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_assertion wasDerivedFrom lhgdn-20090331 NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_provenance.
- NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_assertion wasGeneratedBy ECO_0000203 NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP213197.RAeNXDIt6IMSeRKiTznjPnPhqIsZI0eWhJAAxyCxX3_UI130_provenance.