Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_provenance.
- NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_assertion description "[We sequenced all the mutations as well as coding sequence regions of the 12 genes in an independent sample set including 35 medullary thyroid cancers (20 MEN2A) and 34 PCCs (22 MEN2A), but found no recurrent mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_provenance.
- NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_assertion evidence source_evidence_literature NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_provenance.
- NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_assertion SIO_000772 25404689 NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_provenance.
- NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_assertion wasDerivedFrom befree-2016 NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_provenance.
- NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_assertion wasGeneratedBy ECO_0000203 NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_provenance.