Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_provenance.
- NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_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." NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_provenance.
- NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_assertion evidence source_evidence_literature NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_provenance.
- NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_assertion SIO_000772 17605401 NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_provenance.
- NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_assertion wasDerivedFrom gad-20130706 NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_provenance.
- NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_assertion wasGeneratedBy ECO_0000203 NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_provenance.
- gad-20130706 importedOn "2013-07-06" NP52293.RAA8IhD8fkPtbn7dyzB4GvBw115B5Ptd-pjB9WwwNoWEg130_provenance.