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- NP621335.RA4lyC_x_pwdehZaTIWR3Etodb2HMstB9f195EvALSePM130_assertion type Assertion NP621335.RA4lyC_x_pwdehZaTIWR3Etodb2HMstB9f195EvALSePM130_head.
- NP621335.RA4lyC_x_pwdehZaTIWR3Etodb2HMstB9f195EvALSePM130_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." NP621335.RA4lyC_x_pwdehZaTIWR3Etodb2HMstB9f195EvALSePM130_provenance.
- NP621335.RA4lyC_x_pwdehZaTIWR3Etodb2HMstB9f195EvALSePM130_assertion evidence source_evidence_literature NP621335.RA4lyC_x_pwdehZaTIWR3Etodb2HMstB9f195EvALSePM130_provenance.
- NP621335.RA4lyC_x_pwdehZaTIWR3Etodb2HMstB9f195EvALSePM130_assertion SIO_000772 17646629 NP621335.RA4lyC_x_pwdehZaTIWR3Etodb2HMstB9f195EvALSePM130_provenance.
- NP621335.RA4lyC_x_pwdehZaTIWR3Etodb2HMstB9f195EvALSePM130_assertion wasDerivedFrom befree-2016 NP621335.RA4lyC_x_pwdehZaTIWR3Etodb2HMstB9f195EvALSePM130_provenance.
- NP621335.RA4lyC_x_pwdehZaTIWR3Etodb2HMstB9f195EvALSePM130_assertion wasGeneratedBy ECO_0000203 NP621335.RA4lyC_x_pwdehZaTIWR3Etodb2HMstB9f195EvALSePM130_provenance.