Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_provenance.
- NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_assertion description "[Finally, we show that the previously generated mouse model of Spg7-linked hereditary spastic paraplegia is an isoform-specific knock-out, in which mitochondrial paraplegin is specifically ablated, while expression of paraplegin-2 is retained.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_provenance.
- NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_assertion evidence source_evidence_literature NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_provenance.
- NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_assertion SIO_000772 22563492 NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_provenance.
- NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_assertion wasDerivedFrom befree-20140225 NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_provenance.
- NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_assertion wasGeneratedBy ECO_0000203 NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP671621.RAv--zXzJJZgrKme4hv94rzepj7pu7dzkChRM7P1xBynE130_provenance.