Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_provenance.
- NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_assertion description "[A homozygous mutation in LYRM7/MZM1L associated with early onset encephalopathy, lactic acidosis, and severe reduction of mitochondrial complex III activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_provenance.
- NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_assertion evidence source_evidence_literature NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_provenance.
- NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_assertion SIO_000772 24014394 NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_provenance.
- NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_assertion wasDerivedFrom befree-2016 NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_provenance.
- NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_assertion wasGeneratedBy ECO_0000203 NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_provenance.