Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_provenance.
- NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_assertion description "[DYT16 dystonia is a novel recessive form of EO-PD, recently described in few patients, caused by mutations in the PRKRA gene located at chromosome 2q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_provenance.
- NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_assertion evidence source_evidence_literature NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_provenance.
- NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_assertion SIO_000772 19157930 NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_provenance.
- NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_assertion wasDerivedFrom befree-20140225 NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_provenance.
- NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_assertion wasGeneratedBy ECO_0000203 NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP907369.RAXDYI5pI25_u1IyYmIk55cIf3SBc-CsxM0ddXO3LvyCI130_provenance.