Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_assertion> ?p ?o ?g. }
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- NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_assertion type Assertion NP1259188.RATkGieiKcEW1sK6bWtgc2_J2N1RY6gST1Q4kC3UIx0HU130_head.
- 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.