Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_provenance.
- NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_assertion description "[We have found a single 4p+ chromosomal abnormality, 46,XX, -4, +der(4)t(3;4)(q13.3;p16), in a patient with an unusual B cell leukemia of mature phenotype characterized by a high white cell count, tartrate-resistant acid phosphatase-positive malignant cells, splenic white pulp proliferation, and a serum IgM monoclonal gammopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_provenance.
- NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_assertion evidence source_evidence_literature NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_provenance.
- NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_assertion SIO_000772 2548046 NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_provenance.
- NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_assertion wasDerivedFrom befree-20140225 NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_provenance.
- NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_assertion wasGeneratedBy ECO_0000203 NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP833785.RA78W2mc2ZTvl86-j5Z7nZmCEL1FA9ar5hDckbObnCxLk130_provenance.