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- source_evidence_literature type ECO_0000212 NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_provenance.
- NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_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." NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_provenance.
- NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_assertion evidence source_evidence_literature NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_provenance.
- NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_assertion SIO_000772 22329956 NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_provenance.
- NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_assertion wasDerivedFrom befree-2016 NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_provenance.
- NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_assertion wasGeneratedBy ECO_0000203 NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_provenance.
- befree-2016 importedOn "2016-02-19" NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_provenance.