Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_provenance.
- NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_assertion description "[Screening of the orexin signaling system detected a 408 isoleucine to valine mutation in HCRTR1 that showed significant genotypic association with polydipsic-hyponatremic schizophrenia (p = .012).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_provenance.
- NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_assertion evidence source_evidence_literature NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_provenance.
- NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_assertion SIO_000772 15978554 NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_provenance.
- NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_assertion wasDerivedFrom befree-2016 NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_provenance.
- NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_assertion wasGeneratedBy ECO_0000203 NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_provenance.
- befree-2016 importedOn "2016-02-19" NP500924.RAalF0QeCtRO6tzk32S9Mqam7HahrL02e4T0PH4WMUUIY130_provenance.