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- NP945138.RA-Y9oWg1A3GeRrP48XZTqWxSQf0AWk__JNe-8GqfqDo0130_assertion type Assertion NP945138.RA-Y9oWg1A3GeRrP48XZTqWxSQf0AWk__JNe-8GqfqDo0130_head.
- NP945138.RA-Y9oWg1A3GeRrP48XZTqWxSQf0AWk__JNe-8GqfqDo0130_assertion wasGeneratedBy ECO_0000203 NP945138.RA-Y9oWg1A3GeRrP48XZTqWxSQf0AWk__JNe-8GqfqDo0130_provenance.
- NP945138.RA-Y9oWg1A3GeRrP48XZTqWxSQf0AWk__JNe-8GqfqDo0130_assertion wasDerivedFrom befree-20150227 NP945138.RA-Y9oWg1A3GeRrP48XZTqWxSQf0AWk__JNe-8GqfqDo0130_provenance.
- NP945138.RA-Y9oWg1A3GeRrP48XZTqWxSQf0AWk__JNe-8GqfqDo0130_assertion SIO_000772 22461326 NP945138.RA-Y9oWg1A3GeRrP48XZTqWxSQf0AWk__JNe-8GqfqDo0130_provenance.
- NP945138.RA-Y9oWg1A3GeRrP48XZTqWxSQf0AWk__JNe-8GqfqDo0130_assertion evidence source_evidence_literature NP945138.RA-Y9oWg1A3GeRrP48XZTqWxSQf0AWk__JNe-8GqfqDo0130_provenance.
- NP945138.RA-Y9oWg1A3GeRrP48XZTqWxSQf0AWk__JNe-8GqfqDo0130_assertion description "[Although this study does not provide irrefutable evidence that GALNT12 variants are highly penetrant alleles that predispose to CRC in the majority of unexplained hereditary CRC families, it does provide additional evidence to support an important role of these variants in a proportion of this considerable high-risk group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945138.RA-Y9oWg1A3GeRrP48XZTqWxSQf0AWk__JNe-8GqfqDo0130_provenance.