Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_provenance.
- NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_assertion description "[Peripheral blood samples from 146 prospectively enrolled patients were used for genotyping polymorphisms in thymidylate synthase (TS), methylenetetrahydrofolate reductase (MTHFR), excision repair cross-complementation group-1 (ERCC 1) xeroderma pigmentosum group-D (XPD), X-ray cross-complementing-1 (XRCC 1), X-ray cross-complementing-3 (XRCC 3) and uridine diphosphate-glucuronosyltransferases-A1 (UGT1 A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_provenance.
- NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_assertion evidence source_evidence_literature NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_provenance.
- NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_assertion SIO_000772 17549067 NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_provenance.
- NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_assertion wasDerivedFrom befree-20140225 NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_provenance.
- NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_assertion wasGeneratedBy ECO_0000203 NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP723957.RAdaPvryR9SYfYXqbbWLu1lPU3mIKiTVrOr3Lqi49fMHA130_provenance.