Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_provenance.
- NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_assertion description "[The findings of these studies have indicated the presence of rare, high-penetrance alleles with large effects, such as CDKN2A and CDK4, more common, moderately penetrant genes like MC1R, and very common, low-penetrance polymorphisms with small effects that are related to pigmentation, nevus count, immune responses, DNA repair, metabolism, and the vitamin D receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_provenance.
- NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_assertion evidence source_evidence_literature NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_provenance.
- NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_assertion SIO_000772 22583682 NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_provenance.
- NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_assertion wasDerivedFrom befree-20140225 NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_provenance.
- NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_assertion wasGeneratedBy ECO_0000203 NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP939931.RAJi5BXYPnWXarmejY1wMYa_I6c70Wa7bvJ_u657a0m-A130_provenance.