Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_provenance.
- NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_assertion description "[The recurring chromosomal 9;11 translocation [t(9;11) (p22;q23)] typically is associated with acute monoblastic leukemia, but a number of patients with acute lymphoblastic leukemia also have been reported to have the t(9;11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_provenance.
- NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_assertion evidence source_evidence_literature NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_provenance.
- NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_assertion SIO_000772 1906342 NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_provenance.
- NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_assertion wasDerivedFrom befree-20140225 NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_provenance.
- NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_assertion wasGeneratedBy ECO_0000203 NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP937501.RAFeH4a0b3i70tyOAKP7erW58rcnRVl3lEuiAjrom1wa4130_provenance.