Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_provenance.
- NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_assertion description "[RET genetic screening of patients with apparently sporadic MTC represents a major tool for the preclinical diagnosis and early treatment of unsuspected affected family members and allows the identification of a relevant percentage of hidden FMTC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_provenance.
- NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_assertion evidence source_evidence_literature NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_provenance.
- NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_assertion SIO_000772 21054478 NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_provenance.
- NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_assertion wasDerivedFrom befree-2016 NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_provenance.
- NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_assertion wasGeneratedBy ECO_0000203 NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_provenance.
- befree-2016 importedOn "2016-02-19" NP850683.RABdEq-XX82tla6E7a3RpFDGdnidoyZ6xjx9g0k_JyYR0130_provenance.