Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_provenance.
- NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_assertion description "[Change in the spectrum of RET mutations diagnosed between 1994 and 2006]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_provenance.
- NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_assertion evidence source_evidence_literature NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_provenance.
- NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_assertion SIO_000772 17605401 NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_provenance.
- NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_assertion wasDerivedFrom gad-20150221 NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_provenance.
- NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_assertion wasGeneratedBy ECO_0000203 NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP108711.RAaECZ1hVnDgIg22I54QFTpEOKk-Sj9_ACmcI6No6-PdA130_provenance.