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- source_evidence_literature type ECO_0000212 NP710193.RAVG5Ch294HkNpdI1QGxyGFc6HAoT2G914VjcForwiF0s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710193.RAVG5Ch294HkNpdI1QGxyGFc6HAoT2G914VjcForwiF0s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710193.RAVG5Ch294HkNpdI1QGxyGFc6HAoT2G914VjcForwiF0s130_provenance.
- NP710193.RAVG5Ch294HkNpdI1QGxyGFc6HAoT2G914VjcForwiF0s130_assertion description "[A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710193.RAVG5Ch294HkNpdI1QGxyGFc6HAoT2G914VjcForwiF0s130_provenance.
- NP710193.RAVG5Ch294HkNpdI1QGxyGFc6HAoT2G914VjcForwiF0s130_assertion evidence source_evidence_literature NP710193.RAVG5Ch294HkNpdI1QGxyGFc6HAoT2G914VjcForwiF0s130_provenance.
- NP710193.RAVG5Ch294HkNpdI1QGxyGFc6HAoT2G914VjcForwiF0s130_assertion SIO_000772 17646629 NP710193.RAVG5Ch294HkNpdI1QGxyGFc6HAoT2G914VjcForwiF0s130_provenance.
- NP710193.RAVG5Ch294HkNpdI1QGxyGFc6HAoT2G914VjcForwiF0s130_assertion wasDerivedFrom befree-20150227 NP710193.RAVG5Ch294HkNpdI1QGxyGFc6HAoT2G914VjcForwiF0s130_provenance.
- NP710193.RAVG5Ch294HkNpdI1QGxyGFc6HAoT2G914VjcForwiF0s130_assertion wasGeneratedBy ECO_0000203 NP710193.RAVG5Ch294HkNpdI1QGxyGFc6HAoT2G914VjcForwiF0s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710193.RAVG5Ch294HkNpdI1QGxyGFc6HAoT2G914VjcForwiF0s130_provenance.