Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_provenance.
- NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_assertion description "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_provenance.
- NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_assertion evidence source_evidence_literature NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_provenance.
- NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_assertion SIO_000772 22442086 NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_provenance.
- NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_assertion wasDerivedFrom befree-20140225 NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_provenance.
- NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_assertion wasGeneratedBy ECO_0000203 NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212187.RABQ1wN00Du04S6M27KVFxD9s3T5DRrP23rNGA0p6Qf3I130_provenance.