Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_provenance.
- NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_assertion description "[It seems likely that this technology will also have an impact on the management of sporadic MTC, although it is still too early to define a specific role for mutational analysis in these patients, except to exclude hereditary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_provenance.
- NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_assertion evidence source_evidence_literature NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_provenance.
- NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_assertion SIO_000772 7575334 NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_provenance.
- NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_assertion wasDerivedFrom befree-20140225 NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_provenance.
- NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_assertion wasGeneratedBy ECO_0000203 NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP691337.RAV1CCHLx4x_i-0nFDIEntjGDRdoPwp8CArhqgPVPh-T4130_provenance.