Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_assertion> ?p ?o ?g. }
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- NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_assertion type Assertion NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_head.
- NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_assertion description "[The TYR haplotype carrying only the Arg402Gln variant allele was significantly associated with SCC risk (OR, 1.35; 95% CI, 1.04-1.74).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_provenance.
- NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_assertion evidence source_evidence_literature NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_provenance.
- NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_assertion SIO_000772 19384953 NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_provenance.
- NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_assertion wasDerivedFrom befree-20150227 NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_provenance.
- NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_assertion wasGeneratedBy ECO_0000203 NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_provenance.