Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_provenance.
- NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_assertion description "[Although all patients displayed a BII/common phenotype, supernumerary Ph and trisomy 8 were associated with higher expression of CD19 and CD22 and of CD19, CD34, CD45, and HLA-DR, respectively; in turn, cases with monosomy 7 showed lower CD19, CD22, CD34, and cCD79a and del(9p21)(+) blasts were CD13(-) and CD33(-).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_provenance.
- NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_assertion evidence source_evidence_literature NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_provenance.
- NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_assertion SIO_000772 15789066 NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_provenance.
- NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_assertion wasDerivedFrom befree-20140225 NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_provenance.
- NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_assertion wasGeneratedBy ECO_0000203 NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP711649.RACWGSQbLbiGNMpJu7Q0ORIxN5Z8X2mLfse1shI99KxYg130_provenance.