Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_provenance.
- NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_assertion description "[We now report the cloning of a t(12;21) translocation breakpoint involving 12p13 and 21q22 in two cases of childhood pre-B acute lymphoblastic leukemia, in which t(12;21) rearrangements were not initially apparent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_provenance.
- NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_assertion evidence source_evidence_literature NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_provenance.
- NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_assertion SIO_000772 7761424 NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_provenance.
- NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_assertion wasDerivedFrom befree-20140225 NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_provenance.
- NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_assertion wasGeneratedBy ECO_0000203 NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_provenance.
- befree-20140225 importedOn "2014-02-25" NP868177.RA_WsuXm0S7Uts1QTuDwYNWU7j5r7lorb-QRICCmez0ls130_provenance.