Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_provenance.
- NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_assertion description "[Mutations in the Senataxin gene (SETX) are associated with autosomal recessive ataxia-ocular apraxia 2 (AOA2) and autosomal dominant juvenile ALS (ALS4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_provenance.
- NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_assertion evidence source_evidence_literature NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_provenance.
- NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_assertion SIO_000772 16717225 NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_provenance.
- NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_assertion wasDerivedFrom befree-2016 NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_provenance.
- NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_assertion wasGeneratedBy ECO_0000203 NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_provenance.
- befree-2016 importedOn "2016-02-19" NP550907.RAr0b1Fl0C8PibHz82j7MFo7GDXjS6RWHjB9jd8Y2KBD0130_provenance.