Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_provenance.
- NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_assertion description "[The results support the concept that deletions as well as depletion of mtDNA are involved in the pathogenesis of Alpers-Huttenlocher syndrome and add 3 new POLG1 mutations associated with an early-onset neurodegenerative disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_provenance.
- NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_assertion evidence source_evidence_literature NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_provenance.
- NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_assertion SIO_000772 16896309 NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_provenance.
- NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_assertion wasDerivedFrom lhgdn-20090331 NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_provenance.
- NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_assertion wasGeneratedBy ECO_0000203 NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP199196.RA0vbAlerIJ14ITLYP4FQom2O1hOddqXdiHGB54DLioNQ130_provenance.