Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_provenance.
- NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_assertion description "[A novel DAX1 (NR0B1) gene mutation was detected in a Turkish newborn boy presenting with primary adrenal insufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_provenance.
- NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_assertion evidence source_evidence_literature NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_provenance.
- NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_assertion SIO_000772 18604556 NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_provenance.
- NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_assertion wasDerivedFrom befree-20140225 NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_provenance.
- NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_assertion wasGeneratedBy ECO_0000203 NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP658497.RA_uViQNHri_hZPiYiIFInE6qELnR_9KBROlWtuVEokRo130_provenance.