Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_provenance.
- NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_assertion description "[However, we did not find any mutations in the PNPLA6 gene in 88 patients with autosomal recessive hereditary spastic paraplegia (ARHSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_provenance.
- NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_assertion evidence source_evidence_literature NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_provenance.
- NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_assertion SIO_000772 25631098 NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_provenance.
- NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_assertion wasDerivedFrom befree-2016 NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_provenance.
- NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_assertion wasGeneratedBy ECO_0000203 NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_provenance.