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- source_evidence_literature type ECO_0000212 NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_provenance.
- NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_assertion description "[19 adults with known mitochondrial mutation (MT) have been assessed with the Stanford Health Assessment Questionnaire 20-item Disability Index (HAQ-DI), the Symptom Check List-90-Revised (SCL-90-R), the Beck Depression Inventory-Short Form (BDI-SF), the Hamilton Depression Rating Scale (HDRS) and the clinical version of the Structured Clinical Interview for the the DSM-IV (SCID-I and SCID-II) As control, 10 patients with hereditary sensorimotor neuropathy (HN), harboring the peripheral myelin protein-22 (PMP22) mutation were examined with the same tools.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_provenance.
- NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_assertion evidence source_evidence_literature NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_provenance.
- NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_assertion SIO_000772 22329956 NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_provenance.
- NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_assertion wasDerivedFrom befree-20150227 NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_provenance.
- NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_assertion wasGeneratedBy ECO_0000203 NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_provenance.
- befree-20150227 importedOn "2015-02-27" NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_provenance.