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- source_evidence_literature type ECO_0000212 NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_provenance.
- NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_assertion description "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_provenance.
- NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_assertion evidence source_evidence_literature NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_provenance.
- NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_assertion SIO_000772 17646629 NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_provenance.
- NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_assertion wasDerivedFrom befree-20150227 NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_provenance.
- NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_assertion wasGeneratedBy ECO_0000203 NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_provenance.