Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_provenance.
- befree-2016 importedOn "2016-02-19" NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_provenance.
- NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_assertion wasGeneratedBy ECO_0000203 NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_provenance.
- NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_assertion wasDerivedFrom befree-2016 NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_provenance.
- NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_assertion SIO_000772 24344687 NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_provenance.
- NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_assertion evidence source_evidence_literature NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_provenance.
- NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_assertion description "[In this study we have identified novel YARS2 mutations and noted marked phenotypic variability among YARS2 MLASA patients, with phenotypes ranging from mild to lethal, and we suggest that the background mtDNA haplotype may be contributing to the phenotypic variability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1137488.RAn37JQOa3gsnJbUYy18yH-XsBqoMMq4xFXAzCKqvMdas130_provenance.