Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_provenance.
- NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_assertion description "[In particular, ASXL1 mutations are common in patients with hematologic malignancies associated with myelodysplasia, including myelodysplastic syndromes (MDSs), and chronic myelomonocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_provenance.
- NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_assertion evidence source_evidence_literature NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_provenance.
- NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_assertion SIO_000772 24216483 NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_provenance.
- NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_assertion wasDerivedFrom befree-20140225 NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_provenance.
- NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_assertion wasGeneratedBy ECO_0000203 NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP481632.RAMv29CXSEnoUG3O-9w2vSxPxqFnQZAybudlVX0VJVTO4130_provenance.