Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_provenance.
- NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_assertion wasGeneratedBy ECO_0000203 NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_provenance.
- NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_assertion wasDerivedFrom befree-20140225 NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_provenance.
- NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_assertion SIO_000772 21294243 NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_provenance.
- NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_assertion evidence source_evidence_literature NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_provenance.
- NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_assertion description "[Therefore we made a decision to screen patients with pediatric myeloid neoplasias for the presence of RUNX1 mutations in their samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP886232.RAyWQRWMUvJoe52WAlbw3pP1KQicyQPfsw2dxZuhPo6bQ130_provenance.