Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_provenance.
- NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_assertion description "[The interstitial deletion at 1p32 involving SIL (SCL-interrupting locus)/SCL (stem cell leukemia) is a case involving two non-V(D)J sites that have been suggested to be V(D)J recombination mistakes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_provenance.
- NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_assertion evidence source_evidence_literature NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_provenance.
- NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_assertion SIO_000772 11390401 NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_provenance.
- NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_assertion wasDerivedFrom befree-20140225 NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_provenance.
- NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_assertion wasGeneratedBy ECO_0000203 NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP686475.RAPXHjX-r2lOp3bAE1n_3HyJCRB71lF3tVAessN26DN-E130_provenance.