Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_provenance.
- NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_assertion description "[Our findings indicate that repeat expansion in C9ORF72 is a major cause of both FTD and ALS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_provenance.
- NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_assertion evidence source_evidence_literature NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_provenance.
- NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_assertion SIO_000772 21944778 NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_provenance.
- NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_assertion wasDerivedFrom befree-2016 NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_provenance.
- NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_assertion wasGeneratedBy ECO_0000203 NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_provenance.
- befree-2016 importedOn "2016-02-19" NP926128.RAf4IZFZTTQHmBDWs46C6VuOi3jxZYaTxeOgRRipGvvFg130_provenance.