Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_provenance.
- NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_assertion description "[Single nucleotide polymorphisms (SNPs) in GSTP1 and copy number variants in GSTM1 and GSTT1 may be candidate low-penetrance variants with a role in susceptibility to malignant melanoma (MM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_provenance.
- NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_assertion evidence source_evidence_literature NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_provenance.
- NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_assertion SIO_000772 22251241 NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_provenance.
- NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_assertion wasDerivedFrom befree-20140225 NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_provenance.
- NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_assertion wasGeneratedBy ECO_0000203 NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP470508.RAd5UgNedV7nk0MLcBCnXoiKGTyJZMeIDCPCF41DishKs130_provenance.