Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_provenance.
- NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_assertion description "[The associated variants at the 1q21.3 locus span a region with ten genes, and plausible candidate genes for melanoma susceptibility include ARNT and SETDB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_provenance.
- NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_assertion evidence source_evidence_literature NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_provenance.
- NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_assertion SIO_000772 21983785 NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_provenance.
- NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_assertion wasDerivedFrom befree-2016 NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_provenance.
- NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_assertion wasGeneratedBy ECO_0000203 NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_provenance.
- befree-2016 importedOn "2016-02-19" NP929519.RAmN_yysDdFK1xX35I9Wr98-Nf_irl1lF-40e9kjTF_XE130_provenance.