Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_assertion type Assertion NP1108565.RAv9U1HL0t-fxfdTGezP8qzSXyN-VRVD2Iz8ZUpV9Nnkw130_head.
- 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.