Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_provenance.
- NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_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." NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_provenance.
- NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_assertion evidence source_evidence_literature NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_provenance.
- NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_assertion SIO_000772 22251241 NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_provenance.
- NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_assertion wasDerivedFrom befree-2016 NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_provenance.
- NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_assertion wasGeneratedBy ECO_0000203 NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_provenance.
- befree-2016 importedOn "2016-02-19" NP953818.RAaWsVo87HyIbE9358AxoBpAprAHRrEDQ0HRhVLv1mM84130_provenance.