Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_provenance.
- NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_assertion description "[Mutations of the aprataxin (APTX) gene cause early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH), also called ataxia with oculomotor apraxia type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_provenance.
- NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_assertion evidence source_evidence_literature NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_provenance.
- NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_assertion SIO_000772 17049295 NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_provenance.
- NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_assertion wasDerivedFrom befree-20140225 NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_provenance.
- NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_assertion wasGeneratedBy ECO_0000203 NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP347274.RAoLKuPB8tPBhnmedKNAcQ9QLTAtUXM845AQhWcm3zvSk130_provenance.