Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_provenance.
- NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_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." NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_provenance.
- NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_assertion evidence source_evidence_literature NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_provenance.
- NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_assertion SIO_000772 15978554 NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_provenance.
- NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_assertion wasDerivedFrom befree-20150227 NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_provenance.
- NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_assertion wasGeneratedBy ECO_0000203 NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP445259.RArpCg1s7fZUqvWaddMiPxI8ATQtza6l6d4iNKMrHrpJg130_provenance.