Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP428927.RA8c676HxZQJ_PrZxJWKadROGvmkXqZcmr7_bzolS3DjQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP428927.RA8c676HxZQJ_PrZxJWKadROGvmkXqZcmr7_bzolS3DjQ130_assertion type Assertion NP428927.RA8c676HxZQJ_PrZxJWKadROGvmkXqZcmr7_bzolS3DjQ130_head.
- NP428927.RA8c676HxZQJ_PrZxJWKadROGvmkXqZcmr7_bzolS3DjQ130_assertion description "[A haplotype near ASIP, known to affect a similar spectrum of pigmentation traits as MC1R variants, conferred significant risk of CM (odds ratio (OR) = 1.45, P = 1.2 x 10(-9)) and BCC (OR = 1.33, P = 1.2 x 10(-6)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428927.RA8c676HxZQJ_PrZxJWKadROGvmkXqZcmr7_bzolS3DjQ130_provenance.
- NP428927.RA8c676HxZQJ_PrZxJWKadROGvmkXqZcmr7_bzolS3DjQ130_assertion evidence source_evidence_literature NP428927.RA8c676HxZQJ_PrZxJWKadROGvmkXqZcmr7_bzolS3DjQ130_provenance.
- NP428927.RA8c676HxZQJ_PrZxJWKadROGvmkXqZcmr7_bzolS3DjQ130_assertion SIO_000772 18488027 NP428927.RA8c676HxZQJ_PrZxJWKadROGvmkXqZcmr7_bzolS3DjQ130_provenance.
- NP428927.RA8c676HxZQJ_PrZxJWKadROGvmkXqZcmr7_bzolS3DjQ130_assertion wasDerivedFrom befree-20140225 NP428927.RA8c676HxZQJ_PrZxJWKadROGvmkXqZcmr7_bzolS3DjQ130_provenance.
- NP428927.RA8c676HxZQJ_PrZxJWKadROGvmkXqZcmr7_bzolS3DjQ130_assertion wasGeneratedBy ECO_0000203 NP428927.RA8c676HxZQJ_PrZxJWKadROGvmkXqZcmr7_bzolS3DjQ130_provenance.