Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_provenance.
- NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_assertion description "[Our findings indicate that variant t(2;11)(p11;q13) does not typify a classical MCL but possibly a more indolent leukemic lymphoma originating from an antigen experienced (mutated) B cell.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_provenance.
- NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_assertion evidence source_evidence_literature NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_provenance.
- NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_assertion SIO_000772 15306823 NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_provenance.
- NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_assertion wasDerivedFrom befree-20140225 NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_provenance.
- NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_assertion wasGeneratedBy ECO_0000203 NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP336641.RAbIblPhGAD1PaiJPAo3KURLUgkzJMW4fS2N97Hl0kJbs130_provenance.