Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_provenance.
- NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_assertion description "[Acquired somatic mutations in ATRX, an X-linked gene encoding a chromatin-associated protein, were recently identified in 4 patients with the rare subtype of myelodysplastic syndrome (MDS) associated with thalassemia (ATMDS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_provenance.
- NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_assertion evidence source_evidence_literature NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_provenance.
- NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_assertion SIO_000772 14592816 NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_provenance.
- NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_assertion wasDerivedFrom befree-20140225 NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_provenance.
- NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_assertion wasGeneratedBy ECO_0000203 NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP769754.RAudTbL0oYq0w2l1tXK7sYxElUPcnpRIjySdGBqheiHpw130_provenance.