Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_provenance.
- NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_assertion description "[Translocations involving the HRX/ALL1 locus at chromosomal region 11q23 are among the most frequent cytogenetic abnormalities in acute leukemias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_provenance.
- NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_assertion evidence source_evidence_literature NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_provenance.
- NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_assertion SIO_000772 9041173 NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_provenance.
- NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_assertion wasDerivedFrom befree-20150227 NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_provenance.
- NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_assertion wasGeneratedBy ECO_0000203 NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1014197.RArIUQg776xT-LPRfhTMLesS4SHr5FNHo1URC3s1e4ilU130_provenance.