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- NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_assertion type Assertion NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_head.
- NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_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.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance.
- NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_assertion evidence source_evidence_literature NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance.
- NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_assertion SIO_000772 17646629 NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance.
- NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_assertion wasDerivedFrom lhgdn-20090331 NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance.
- NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_assertion wasGeneratedBy ECO_0000203 NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance.