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- source_evidence_literature type ECO_0000212 NP136903.RAAXCZDNdK2WDEPEHEGPclk90EMSw4NW9Z295R4uXLUYs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP136903.RAAXCZDNdK2WDEPEHEGPclk90EMSw4NW9Z295R4uXLUYs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP136903.RAAXCZDNdK2WDEPEHEGPclk90EMSw4NW9Z295R4uXLUYs130_provenance.
- NP136903.RAAXCZDNdK2WDEPEHEGPclk90EMSw4NW9Z295R4uXLUYs130_assertion description "[A total of 77 polymorphisms in genes related to serotonin synthesis (TPH2), signaling (HTR1A, HTR1E, HTR2A, HTR2B, HTR2C, HTR3A, HTR3B, HTR4, HTR5A, HTR6, and HTR7), transport (SLC6A4), and catabolism (MAOA) were examined in 137 clinically evaluated subjects (40 CFS, 55 with insufficient fatigue, and 42 non-fatigued, NF, controls) derived from a population-based CFS surveillance study in Wichita, Kansas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136903.RAAXCZDNdK2WDEPEHEGPclk90EMSw4NW9Z295R4uXLUYs130_provenance.
- NP136903.RAAXCZDNdK2WDEPEHEGPclk90EMSw4NW9Z295R4uXLUYs130_assertion evidence source_evidence_literature NP136903.RAAXCZDNdK2WDEPEHEGPclk90EMSw4NW9Z295R4uXLUYs130_provenance.
- NP136903.RAAXCZDNdK2WDEPEHEGPclk90EMSw4NW9Z295R4uXLUYs130_assertion SIO_000772 18079067 NP136903.RAAXCZDNdK2WDEPEHEGPclk90EMSw4NW9Z295R4uXLUYs130_provenance.
- NP136903.RAAXCZDNdK2WDEPEHEGPclk90EMSw4NW9Z295R4uXLUYs130_assertion wasDerivedFrom gad-20150221 NP136903.RAAXCZDNdK2WDEPEHEGPclk90EMSw4NW9Z295R4uXLUYs130_provenance.
- NP136903.RAAXCZDNdK2WDEPEHEGPclk90EMSw4NW9Z295R4uXLUYs130_assertion wasGeneratedBy ECO_0000203 NP136903.RAAXCZDNdK2WDEPEHEGPclk90EMSw4NW9Z295R4uXLUYs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP136903.RAAXCZDNdK2WDEPEHEGPclk90EMSw4NW9Z295R4uXLUYs130_provenance.