Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_provenance.
- NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_assertion description "[Asxl1(+/-) mice also developed mild MDS-like disease, which could progress to MDS/myeloproliferative neoplasm, demonstrating a haploinsufficient effect of Asxl1 in the pathogenesis of myeloid malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_provenance.
- NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_assertion evidence source_evidence_literature NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_provenance.
- NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_assertion SIO_000772 24255920 NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_provenance.
- NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_assertion wasDerivedFrom befree-20150227 NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_provenance.
- NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_assertion wasGeneratedBy ECO_0000203 NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978549.RAWpdtDdIw5MvFkC-7Wg5OjvCK1VyA2Cw4qeJfAcPPKUU130_provenance.