Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_provenance.
- NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_assertion description "[Results confirm previously reported associations between the HTR2C 23Ser allele and EPS occurrence and suggest the novel finding of an HTR2C haplotype association with EPS in male chronic schizophrenic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_provenance.
- NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_assertion evidence source_evidence_literature NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_provenance.
- NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_assertion SIO_000772 18205001 NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_provenance.
- NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_assertion wasDerivedFrom gad-20150221 NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_provenance.
- NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_assertion wasGeneratedBy ECO_0000203 NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP136906.RAbx47qvfXiHCsIi09GYoV86xlbISjLKNwmS32jKLDqyc130_provenance.