Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_provenance.
- NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_assertion description "[In male subjects, the variant rs6766410 (p.N163K) located in the HTR3C was significantly associated with OCD (p=0.007).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_provenance.
- NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_assertion evidence source_evidence_literature NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_provenance.
- NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_assertion SIO_000772 23928294 NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_provenance.
- NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_assertion wasDerivedFrom befree-2016 NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_provenance.
- NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_assertion wasGeneratedBy ECO_0000203 NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1100681.RArNy2bmfMo6wfckxDf-8JVI_TpQD9sFSnAaVBViwGWbA130_provenance.