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- source_evidence_literature type ECO_0000212 NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP203911.RAeEIFrXSfqVLmrDVgcwM-DZHzfJOIww2eQAEy_W_OOWY130_provenance.
- 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.