Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1100677.RAh72v33kIJdL8c6NE4m9Myn7-Ec9p03H1kR56hb8dYbk130_assertion> ?p ?o ?g. }
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- NP1100677.RAh72v33kIJdL8c6NE4m9Myn7-Ec9p03H1kR56hb8dYbk130_assertion type Assertion NP1100677.RAh72v33kIJdL8c6NE4m9Myn7-Ec9p03H1kR56hb8dYbk130_head.
- NP1100677.RAh72v33kIJdL8c6NE4m9Myn7-Ec9p03H1kR56hb8dYbk130_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." NP1100677.RAh72v33kIJdL8c6NE4m9Myn7-Ec9p03H1kR56hb8dYbk130_provenance.
- NP1100677.RAh72v33kIJdL8c6NE4m9Myn7-Ec9p03H1kR56hb8dYbk130_assertion evidence source_evidence_literature NP1100677.RAh72v33kIJdL8c6NE4m9Myn7-Ec9p03H1kR56hb8dYbk130_provenance.
- NP1100677.RAh72v33kIJdL8c6NE4m9Myn7-Ec9p03H1kR56hb8dYbk130_assertion SIO_000772 23928294 NP1100677.RAh72v33kIJdL8c6NE4m9Myn7-Ec9p03H1kR56hb8dYbk130_provenance.
- NP1100677.RAh72v33kIJdL8c6NE4m9Myn7-Ec9p03H1kR56hb8dYbk130_assertion wasDerivedFrom befree-2016 NP1100677.RAh72v33kIJdL8c6NE4m9Myn7-Ec9p03H1kR56hb8dYbk130_provenance.
- NP1100677.RAh72v33kIJdL8c6NE4m9Myn7-Ec9p03H1kR56hb8dYbk130_assertion wasGeneratedBy ECO_0000203 NP1100677.RAh72v33kIJdL8c6NE4m9Myn7-Ec9p03H1kR56hb8dYbk130_provenance.