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- NP528667.RA02xwb9-wq9icqgnU1JEszllqd8oNCmqmaHBTAvnVOGY130_assertion type Assertion NP528667.RA02xwb9-wq9icqgnU1JEszllqd8oNCmqmaHBTAvnVOGY130_head.
- NP528667.RA02xwb9-wq9icqgnU1JEszllqd8oNCmqmaHBTAvnVOGY130_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." NP528667.RA02xwb9-wq9icqgnU1JEszllqd8oNCmqmaHBTAvnVOGY130_provenance.
- NP528667.RA02xwb9-wq9icqgnU1JEszllqd8oNCmqmaHBTAvnVOGY130_assertion evidence source_evidence_literature NP528667.RA02xwb9-wq9icqgnU1JEszllqd8oNCmqmaHBTAvnVOGY130_provenance.
- NP528667.RA02xwb9-wq9icqgnU1JEszllqd8oNCmqmaHBTAvnVOGY130_assertion SIO_000772 22329956 NP528667.RA02xwb9-wq9icqgnU1JEszllqd8oNCmqmaHBTAvnVOGY130_provenance.
- NP528667.RA02xwb9-wq9icqgnU1JEszllqd8oNCmqmaHBTAvnVOGY130_assertion wasDerivedFrom befree-20150227 NP528667.RA02xwb9-wq9icqgnU1JEszllqd8oNCmqmaHBTAvnVOGY130_provenance.
- NP528667.RA02xwb9-wq9icqgnU1JEszllqd8oNCmqmaHBTAvnVOGY130_assertion wasGeneratedBy ECO_0000203 NP528667.RA02xwb9-wq9icqgnU1JEszllqd8oNCmqmaHBTAvnVOGY130_provenance.