Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_provenance.
- NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_assertion description "[Genetic analysis of both tumour components showed a distinctive mutational pattern: in the MTC a Cys634Arg substitution in exon 11 of the RET gene and in the two PTC foci a Val600Glu substitution in exon 15 of the BRAF gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_provenance.
- NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_assertion evidence source_evidence_literature NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_provenance.
- NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_assertion SIO_000772 15947103 NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_provenance.
- NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_assertion wasDerivedFrom befree-2016 NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_provenance.
- NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_assertion wasGeneratedBy ECO_0000203 NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_provenance.
- befree-2016 importedOn "2016-02-19" NP498724.RATWfaujYZnUtCbsA8byJEFO2GNlOz3TwVmDGSUKS_H-o130_provenance.