Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP635089.RA-JmLRegipyd77HCU9f3-Aw31I4h0AnJFmpRWLE16pf4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP635089.RA-JmLRegipyd77HCU9f3-Aw31I4h0AnJFmpRWLE16pf4130_assertion type Assertion NP635089.RA-JmLRegipyd77HCU9f3-Aw31I4h0AnJFmpRWLE16pf4130_head.
- NP635089.RA-JmLRegipyd77HCU9f3-Aw31I4h0AnJFmpRWLE16pf4130_assertion description "[A single nucleotide polymorphism variant within the general transcription factor IIH, polypeptide 4 gene, GTF2H4, on chromosome 6p21.33 was significantly associated with MS (odds ratio = 0.7, P = 3.5 x 10(-5)) after accounting for multiple testing and was not due to linkage disequilibrium with HLA-DRB1*1501.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635089.RA-JmLRegipyd77HCU9f3-Aw31I4h0AnJFmpRWLE16pf4130_provenance.
- NP635089.RA-JmLRegipyd77HCU9f3-Aw31I4h0AnJFmpRWLE16pf4130_assertion evidence source_evidence_literature NP635089.RA-JmLRegipyd77HCU9f3-Aw31I4h0AnJFmpRWLE16pf4130_provenance.
- NP635089.RA-JmLRegipyd77HCU9f3-Aw31I4h0AnJFmpRWLE16pf4130_assertion SIO_000772 20522537 NP635089.RA-JmLRegipyd77HCU9f3-Aw31I4h0AnJFmpRWLE16pf4130_provenance.
- NP635089.RA-JmLRegipyd77HCU9f3-Aw31I4h0AnJFmpRWLE16pf4130_assertion wasDerivedFrom befree-20140225 NP635089.RA-JmLRegipyd77HCU9f3-Aw31I4h0AnJFmpRWLE16pf4130_provenance.
- NP635089.RA-JmLRegipyd77HCU9f3-Aw31I4h0AnJFmpRWLE16pf4130_assertion wasGeneratedBy ECO_0000203 NP635089.RA-JmLRegipyd77HCU9f3-Aw31I4h0AnJFmpRWLE16pf4130_provenance.