Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_assertion type Assertion NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_head.
- NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_assertion wasGeneratedBy ECO_0000203 NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_provenance.
- NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_assertion wasDerivedFrom lhgdn-20090331 NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_provenance.
- NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_assertion SIO_000772 12815654 NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_provenance.
- NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_assertion evidence source_evidence_literature NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_provenance.
- NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_assertion description "[We report a novel heterozygous 40 base pair deletion in exon 3 of the parkin gene that increases the susceptibility of carriers to develop parkinsonism/dystonia and manifests variability in regard to age of onset and phenotype in a single family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_provenance.