Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_provenance.
- NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_assertion description "[Mutations in TET2, RUNX1 and JAK2(V617F) are involved in myelodysplastic and/or myeloproliferative syndromes, and more specifically in CMML but were not found in JMML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_provenance.
- NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_assertion evidence source_evidence_literature NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_provenance.
- NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_assertion SIO_000772 20955399 NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_provenance.
- NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_assertion wasDerivedFrom befree-2016 NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_provenance.
- NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_assertion wasGeneratedBy ECO_0000203 NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_provenance.
- befree-2016 importedOn "2016-02-19" NP846452.RAmFbW78WWzpDjUw83F8etBXAo30D21dGy5huym5e2yGc130_provenance.