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- source_evidence_literature type ECO_0000212 NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.
- NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_assertion description "[Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.
- NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_assertion evidence source_evidence_literature NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.
- NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_assertion SIO_000772 21465257 NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.
- NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_assertion wasDerivedFrom befree-20150227 NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.
- NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_assertion wasGeneratedBy ECO_0000203 NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.