Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_provenance.
- NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_assertion wasGeneratedBy ECO_0000203 NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_provenance.
- NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_assertion wasDerivedFrom befree-20150227 NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_provenance.
- NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_assertion SIO_000772 20660572 NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_provenance.
- NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_assertion evidence source_evidence_literature NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_provenance.
- NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_assertion description "[In the NET-Registry, 9/101 patients (8.9%) with ICTs had germline mutations, 8 in MEN1 and 1 in VHL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376354.RAOn1gE4c2C_yUzr1F2ABYECCr6TuAX8VeIIasne1pFfQ130_provenance.