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- source_evidence_literature type ECO_0000212 NP216545.RA50NPGHBFxp_tZyc88si-XN9X2-26n7Wm8TUhAJ3Jrsk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP216545.RA50NPGHBFxp_tZyc88si-XN9X2-26n7Wm8TUhAJ3Jrsk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP216545.RA50NPGHBFxp_tZyc88si-XN9X2-26n7Wm8TUhAJ3Jrsk130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP216545.RA50NPGHBFxp_tZyc88si-XN9X2-26n7Wm8TUhAJ3Jrsk130_provenance.
- NP216545.RA50NPGHBFxp_tZyc88si-XN9X2-26n7Wm8TUhAJ3Jrsk130_assertion wasGeneratedBy ECO_0000203 NP216545.RA50NPGHBFxp_tZyc88si-XN9X2-26n7Wm8TUhAJ3Jrsk130_provenance.
- NP216545.RA50NPGHBFxp_tZyc88si-XN9X2-26n7Wm8TUhAJ3Jrsk130_assertion wasDerivedFrom lhgdn-20090331 NP216545.RA50NPGHBFxp_tZyc88si-XN9X2-26n7Wm8TUhAJ3Jrsk130_provenance.
- NP216545.RA50NPGHBFxp_tZyc88si-XN9X2-26n7Wm8TUhAJ3Jrsk130_assertion SIO_000772 15596607 NP216545.RA50NPGHBFxp_tZyc88si-XN9X2-26n7Wm8TUhAJ3Jrsk130_provenance.
- NP216545.RA50NPGHBFxp_tZyc88si-XN9X2-26n7Wm8TUhAJ3Jrsk130_assertion evidence source_evidence_literature NP216545.RA50NPGHBFxp_tZyc88si-XN9X2-26n7Wm8TUhAJ3Jrsk130_provenance.
- NP216545.RA50NPGHBFxp_tZyc88si-XN9X2-26n7Wm8TUhAJ3Jrsk130_assertion description "[All mutations of atlastin1 in young-onset autosomal dominant spastic paraplegia patients in France were found in exons 7, 8, 12, and 13/exons should be given priority when performing molecular diagnoses for SPG3A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216545.RA50NPGHBFxp_tZyc88si-XN9X2-26n7Wm8TUhAJ3Jrsk130_provenance.