Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_provenance.
- NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_assertion description "[Recent work has identified frequent, recurrent mutations in IDH1 or IDH2 in nearly half of central chondrosarcomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_provenance.
- NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_assertion evidence source_evidence_literature NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_provenance.
- NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_assertion SIO_000772 23770606 NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_provenance.
- NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_assertion wasDerivedFrom befree-20150227 NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_provenance.
- NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_assertion wasGeneratedBy ECO_0000203 NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP475242.RA18ElmvJW7W7NbETElhIC_v4-d4ybYuua6DgFhsGHOj8130_provenance.