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- source_evidence_literature type ECO_0000212 NP452520.RAxxa2iqWLcAsPOB1-956yMsacRKa67dg5a_8lAWtQUFI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP452520.RAxxa2iqWLcAsPOB1-956yMsacRKa67dg5a_8lAWtQUFI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP452520.RAxxa2iqWLcAsPOB1-956yMsacRKa67dg5a_8lAWtQUFI130_provenance.
- NP452520.RAxxa2iqWLcAsPOB1-956yMsacRKa67dg5a_8lAWtQUFI130_assertion description "[Rapid-onset dystonia-parkinsonism (RDP, DYT12) is a distinctive autosomal-dominant movement disorder with variable expressivity and reduced penetrance characterized by abrupt onset of dystonia, usually accompanied by signs of parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452520.RAxxa2iqWLcAsPOB1-956yMsacRKa67dg5a_8lAWtQUFI130_provenance.
- NP452520.RAxxa2iqWLcAsPOB1-956yMsacRKa67dg5a_8lAWtQUFI130_assertion evidence source_evidence_literature NP452520.RAxxa2iqWLcAsPOB1-956yMsacRKa67dg5a_8lAWtQUFI130_provenance.
- NP452520.RAxxa2iqWLcAsPOB1-956yMsacRKa67dg5a_8lAWtQUFI130_assertion SIO_000772 15260953 NP452520.RAxxa2iqWLcAsPOB1-956yMsacRKa67dg5a_8lAWtQUFI130_provenance.
- NP452520.RAxxa2iqWLcAsPOB1-956yMsacRKa67dg5a_8lAWtQUFI130_assertion wasDerivedFrom befree-2016 NP452520.RAxxa2iqWLcAsPOB1-956yMsacRKa67dg5a_8lAWtQUFI130_provenance.
- NP452520.RAxxa2iqWLcAsPOB1-956yMsacRKa67dg5a_8lAWtQUFI130_assertion wasGeneratedBy ECO_0000203 NP452520.RAxxa2iqWLcAsPOB1-956yMsacRKa67dg5a_8lAWtQUFI130_provenance.
- befree-2016 importedOn "2016-02-19" NP452520.RAxxa2iqWLcAsPOB1-956yMsacRKa67dg5a_8lAWtQUFI130_provenance.