Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_provenance.
- NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_assertion description "[Lactate peak, cerebellar and cortical atrophies are consistent with the mitochondrial dysfunction related to OPA1 mutations and might result from widespread neuronal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_provenance.
- NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_assertion evidence source_evidence_literature NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_provenance.
- NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_assertion SIO_000772 25641387 NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_provenance.
- NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_assertion wasDerivedFrom befree-2016 NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_provenance.
- NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_assertion wasGeneratedBy ECO_0000203 NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1260125.RAgsnkTQAMmiLdEC8aEnPhkT3cwae4_1GMuN-MLgIaHpw130_provenance.