Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_provenance.
- NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_assertion description "[Five Duchenne muscular dystrophy -causing mutations in dystrophin gene, 697-698insGT, C616T, G1255T, C4279T, and C2302T, were identified in the new stop codons in downstream sites of mutations, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_provenance.
- NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_assertion evidence source_evidence_literature NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_provenance.
- NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_assertion SIO_000772 16883524 NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_provenance.
- NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_assertion wasDerivedFrom lhgdn-20090331 NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_provenance.
- NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_assertion wasGeneratedBy ECO_0000203 NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP218752.RAO_QAS7FWUPokARBotcjj2xHf-cmDfYQ2EQHNm27wpR0130_provenance.