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- source_evidence_literature type ECO_0000212 NP200177.RADoeDUzCxRh4w7oHDihYrH3XI6l-_bVZEz71rAG7ELjg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP200177.RADoeDUzCxRh4w7oHDihYrH3XI6l-_bVZEz71rAG7ELjg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP200177.RADoeDUzCxRh4w7oHDihYrH3XI6l-_bVZEz71rAG7ELjg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP200177.RADoeDUzCxRh4w7oHDihYrH3XI6l-_bVZEz71rAG7ELjg130_provenance.
- NP200177.RADoeDUzCxRh4w7oHDihYrH3XI6l-_bVZEz71rAG7ELjg130_assertion wasGeneratedBy ECO_0000203 NP200177.RADoeDUzCxRh4w7oHDihYrH3XI6l-_bVZEz71rAG7ELjg130_provenance.
- NP200177.RADoeDUzCxRh4w7oHDihYrH3XI6l-_bVZEz71rAG7ELjg130_assertion wasDerivedFrom lhgdn-20090331 NP200177.RADoeDUzCxRh4w7oHDihYrH3XI6l-_bVZEz71rAG7ELjg130_provenance.
- NP200177.RADoeDUzCxRh4w7oHDihYrH3XI6l-_bVZEz71rAG7ELjg130_assertion SIO_000772 12815654 NP200177.RADoeDUzCxRh4w7oHDihYrH3XI6l-_bVZEz71rAG7ELjg130_provenance.
- NP200177.RADoeDUzCxRh4w7oHDihYrH3XI6l-_bVZEz71rAG7ELjg130_assertion evidence source_evidence_literature NP200177.RADoeDUzCxRh4w7oHDihYrH3XI6l-_bVZEz71rAG7ELjg130_provenance.
- NP200177.RADoeDUzCxRh4w7oHDihYrH3XI6l-_bVZEz71rAG7ELjg130_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." NP200177.RADoeDUzCxRh4w7oHDihYrH3XI6l-_bVZEz71rAG7ELjg130_provenance.