Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_provenance.
- NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_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." NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_provenance.
- NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_assertion evidence source_evidence_literature NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_provenance.
- NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_assertion SIO_000772 18079067 NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_provenance.
- NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_assertion wasDerivedFrom gad-20150221 NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_provenance.
- NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_assertion wasGeneratedBy ECO_0000203 NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP136909.RAPMeqL7ysCvK1Bi_N8E8OothpY10KUQeQotoVBSwg_hc130_provenance.