Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_provenance.
- NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_assertion description "[We now report a change in the spectrum of mutations detected in the RET proto-oncogene in patients with hereditary MTC from the 'classical' mutation at codon 634 in exon 11 (level 2) to more cases with mutations in the exons 13-15 (level 1) and less aggressive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_provenance.
- NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_assertion evidence source_evidence_literature NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_provenance.
- NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_assertion SIO_000772 17605401 NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_provenance.
- NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_assertion wasDerivedFrom befree-2016 NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_provenance.
- NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_assertion wasGeneratedBy ECO_0000203 NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_provenance.
- befree-2016 importedOn "2016-02-19" NP618072.RANMOlRT4C5v9ggLnW-pdNYZCQ4niv2ykx3s0dj-AHoGE130_provenance.