Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_assertion type Assertion NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_head.
- NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_assertion description "[This study enables us to estimate the frequency of the SPG3A mutations in France at 39% in families with young-onset autosomal dominant spastic paraplegia after exclusion of SPG4 cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance.
- NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_assertion evidence source_evidence_literature NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance.
- NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_assertion SIO_000772 15596607 NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance.
- NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_assertion wasDerivedFrom befree-20140225 NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance.
- NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_assertion wasGeneratedBy ECO_0000203 NP708318.RAATlkQI814Qbq52W9XX7w1Xpt5JNUzWL1Ka6XXqTML3A130_provenance.