Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_provenance.
- NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_assertion description "[Ataxia with oculomotor apraxia defines a group of genetically distinct recessive ataxias including ataxia-telangectasia (A-T, ATM gene), ataxia with oculomotor apraxia type 1 (AOA1, APTX gene) and type 2 (AOA2, SETX gene).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_provenance.
- NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_assertion evidence source_evidence_literature NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_provenance.
- NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_assertion SIO_000772 23941260 NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_provenance.
- NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_assertion wasDerivedFrom befree-2016 NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_provenance.
- NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_assertion wasGeneratedBy ECO_0000203 NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1102139.RAYNIwD2R5sQB7giR5coSuteUrBTn8qOTLViAxOIDpVpk130_provenance.