Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_provenance.
- NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_assertion description "[The case-control analyses revealed a nominal significant association of the HTR3D variant rs1000592 (p.H52R) with OCD (p=0.029) which was also evident after combination of the case-control and the trio-results (p=0.024).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_provenance.
- NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_assertion evidence source_evidence_literature NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_provenance.
- NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_assertion SIO_000772 23928294 NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_provenance.
- NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_assertion wasDerivedFrom befree-2016 NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_provenance.
- NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_assertion wasGeneratedBy ECO_0000203 NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1100685.RA4jQnlDbxTzDEPQNbcAh6DBLyp0cgGT0wAMXeAN2AeOY130_provenance.