Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_provenance.
- NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_assertion description "[Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive disorder characterized by early-onset cerebellar ataxia, oculomotor apraxia, and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_provenance.
- NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_assertion evidence source_evidence_literature NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_provenance.
- NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_assertion SIO_000772 15596775 NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_provenance.
- NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_assertion wasDerivedFrom befree-20140225 NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_provenance.
- NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_assertion wasGeneratedBy ECO_0000203 NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP291972.RAHrkWh1oRVtM1slVjeWb-wVTk6Gflc82ZZpWF7WrG3tY130_provenance.