Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_provenance.
- NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_assertion description "[Genomic amplification was detected in 26% and 23% of the ARMS and ERMS cases, respectively (with nearly all of the latter subset exhibiting anaplastic features).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_provenance.
- NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_assertion evidence source_evidence_literature NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_provenance.
- NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_assertion SIO_000772 11807989 NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_provenance.
- NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_assertion wasDerivedFrom befree-2016 NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_provenance.
- NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_assertion wasGeneratedBy ECO_0000203 NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_provenance.
- befree-2016 importedOn "2016-02-19" NP343050.RAo87Ivv2eTOEL3xFKBynXfStH6__Fk3oOP49FOhryRNA130_provenance.