Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_provenance.
- NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_assertion wasGeneratedBy ECO_0000203 NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_provenance.
- NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_assertion wasDerivedFrom befree-20140225 NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_provenance.
- NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_assertion SIO_000772 7520272 NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_provenance.
- NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_assertion evidence source_evidence_literature NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_provenance.
- NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_assertion description "[The deletion 20q in myeloproliferative diseases (MPD), the deletion of 5q and t(1;7) in myelodysplastic syndromes (MDS), and t(3;3) in acute myeloid leukemia subtype M7 (AML-M7) were seen in all or at least in two myeloid lineages.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP582985.RAoFh9_-dEsDxMVqWRHBp6Pt4R6MpeduuhHkKYgQa9hCw130_provenance.