Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_provenance.
- NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_assertion description "[By fusing lymphoblastoid cells of an AGS patient that exhibited a microdeletion in the short arm of Chr 20 encompassing bands p11.23 to p12.3 with rodent thermosensitive mutant cells (CHOtsH1-1) deficient in-leucyl-tRNA synthetase, we isolated a somatic cell hybrid segregating the deleted human Chr 20.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_provenance.
- NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_assertion evidence source_evidence_literature NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_provenance.
- NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_assertion SIO_000772 7873876 NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_provenance.
- NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_assertion wasDerivedFrom befree-20140225 NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_provenance.
- NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_assertion wasGeneratedBy ECO_0000203 NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP882880.RAEMsxRxmBLJmaAK9DttGHJVCqCfFORzjeIjvZcTYw82M130_provenance.