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- source_evidence_literature type ECO_0000212 NP357146.RAnO-5Crd-KZ88ZWPAt4L3f10krrSVeYJ1UrjxRGIq7yo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP357146.RAnO-5Crd-KZ88ZWPAt4L3f10krrSVeYJ1UrjxRGIq7yo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP357146.RAnO-5Crd-KZ88ZWPAt4L3f10krrSVeYJ1UrjxRGIq7yo130_provenance.
- NP357146.RAnO-5Crd-KZ88ZWPAt4L3f10krrSVeYJ1UrjxRGIq7yo130_assertion description "[The giant axonal neuropathy gene was localised by homozygosity mapping to chromosome 16q24.1 and identified as encoding a novel, ubiquitously expressed cytoskeletal protein named gigaxonin.We describe a consanguineous Algerian family with three affected sibs aged 16, 14 and 12 years who present a mild demyelinating sensory motor neuropathy, hypoacousia and kyphoscoliosis which was moderate in the two elder patients, severe in the third one, with no sign of central nervous system involvement and normal cerebral magnetic resonance imaging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357146.RAnO-5Crd-KZ88ZWPAt4L3f10krrSVeYJ1UrjxRGIq7yo130_provenance.
- NP357146.RAnO-5Crd-KZ88ZWPAt4L3f10krrSVeYJ1UrjxRGIq7yo130_assertion evidence source_evidence_literature NP357146.RAnO-5Crd-KZ88ZWPAt4L3f10krrSVeYJ1UrjxRGIq7yo130_provenance.
- NP357146.RAnO-5Crd-KZ88ZWPAt4L3f10krrSVeYJ1UrjxRGIq7yo130_assertion SIO_000772 12398836 NP357146.RAnO-5Crd-KZ88ZWPAt4L3f10krrSVeYJ1UrjxRGIq7yo130_provenance.
- NP357146.RAnO-5Crd-KZ88ZWPAt4L3f10krrSVeYJ1UrjxRGIq7yo130_assertion wasDerivedFrom befree-20150227 NP357146.RAnO-5Crd-KZ88ZWPAt4L3f10krrSVeYJ1UrjxRGIq7yo130_provenance.
- NP357146.RAnO-5Crd-KZ88ZWPAt4L3f10krrSVeYJ1UrjxRGIq7yo130_assertion wasGeneratedBy ECO_0000203 NP357146.RAnO-5Crd-KZ88ZWPAt4L3f10krrSVeYJ1UrjxRGIq7yo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP357146.RAnO-5Crd-KZ88ZWPAt4L3f10krrSVeYJ1UrjxRGIq7yo130_provenance.