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- source_evidence_literature type ECO_0000212 NP953817.RA4aJfnmMyByTB9VC0PeHXfv6SeehUfCao_caRIM-9nw0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP953817.RA4aJfnmMyByTB9VC0PeHXfv6SeehUfCao_caRIM-9nw0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP953817.RA4aJfnmMyByTB9VC0PeHXfv6SeehUfCao_caRIM-9nw0130_provenance.
- NP953817.RA4aJfnmMyByTB9VC0PeHXfv6SeehUfCao_caRIM-9nw0130_assertion description "[In addition, this study is one of the largest GST polymorphism studies undertaken in the Spanish population and the first time that copy number variants have been scrutinized in relation to MM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP953817.RA4aJfnmMyByTB9VC0PeHXfv6SeehUfCao_caRIM-9nw0130_provenance.
- NP953817.RA4aJfnmMyByTB9VC0PeHXfv6SeehUfCao_caRIM-9nw0130_assertion evidence source_evidence_literature NP953817.RA4aJfnmMyByTB9VC0PeHXfv6SeehUfCao_caRIM-9nw0130_provenance.
- NP953817.RA4aJfnmMyByTB9VC0PeHXfv6SeehUfCao_caRIM-9nw0130_assertion SIO_000772 22251241 NP953817.RA4aJfnmMyByTB9VC0PeHXfv6SeehUfCao_caRIM-9nw0130_provenance.
- NP953817.RA4aJfnmMyByTB9VC0PeHXfv6SeehUfCao_caRIM-9nw0130_assertion wasDerivedFrom befree-2016 NP953817.RA4aJfnmMyByTB9VC0PeHXfv6SeehUfCao_caRIM-9nw0130_provenance.
- NP953817.RA4aJfnmMyByTB9VC0PeHXfv6SeehUfCao_caRIM-9nw0130_assertion wasGeneratedBy ECO_0000203 NP953817.RA4aJfnmMyByTB9VC0PeHXfv6SeehUfCao_caRIM-9nw0130_provenance.
- befree-2016 importedOn "2016-02-19" NP953817.RA4aJfnmMyByTB9VC0PeHXfv6SeehUfCao_caRIM-9nw0130_provenance.