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- source_evidence_literature type ECO_0000212 NP136897.RAyHj0cbl29ZPEfORzc0dDu4g1z83kDZsNJAGy7A71-BA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP136897.RAyHj0cbl29ZPEfORzc0dDu4g1z83kDZsNJAGy7A71-BA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP136897.RAyHj0cbl29ZPEfORzc0dDu4g1z83kDZsNJAGy7A71-BA130_provenance.
- NP136897.RAyHj0cbl29ZPEfORzc0dDu4g1z83kDZsNJAGy7A71-BA130_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." NP136897.RAyHj0cbl29ZPEfORzc0dDu4g1z83kDZsNJAGy7A71-BA130_provenance.
- NP136897.RAyHj0cbl29ZPEfORzc0dDu4g1z83kDZsNJAGy7A71-BA130_assertion evidence source_evidence_literature NP136897.RAyHj0cbl29ZPEfORzc0dDu4g1z83kDZsNJAGy7A71-BA130_provenance.
- NP136897.RAyHj0cbl29ZPEfORzc0dDu4g1z83kDZsNJAGy7A71-BA130_assertion SIO_000772 18079067 NP136897.RAyHj0cbl29ZPEfORzc0dDu4g1z83kDZsNJAGy7A71-BA130_provenance.
- NP136897.RAyHj0cbl29ZPEfORzc0dDu4g1z83kDZsNJAGy7A71-BA130_assertion wasDerivedFrom gad-20150221 NP136897.RAyHj0cbl29ZPEfORzc0dDu4g1z83kDZsNJAGy7A71-BA130_provenance.
- NP136897.RAyHj0cbl29ZPEfORzc0dDu4g1z83kDZsNJAGy7A71-BA130_assertion wasGeneratedBy ECO_0000203 NP136897.RAyHj0cbl29ZPEfORzc0dDu4g1z83kDZsNJAGy7A71-BA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP136897.RAyHj0cbl29ZPEfORzc0dDu4g1z83kDZsNJAGy7A71-BA130_provenance.