Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_provenance.
- NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_assertion description "[Overlaps between the diverse disorders were seen also for the JAK2V617F (MPN 66/89; 74%; MDS/MPN 4/14; 29%; MDS 2/63; 3%) and NRAS mutations (MDS 2/67; 3%; MPN 2/4; MDS/MPN 1/1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_provenance.
- NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_assertion evidence source_evidence_literature NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_provenance.
- NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_assertion SIO_000772 19415278 NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_provenance.
- NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_assertion wasDerivedFrom befree-20150227 NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_provenance.
- NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_assertion wasGeneratedBy ECO_0000203 NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP982406.RAA1dkKmwWXpbKYNXvmJHH5nx5hSWq5ese0kb5fSLFxuU130_provenance.