Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_provenance.
- NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_assertion description "[Significant differences in the allele and genotype frequencies between the controls and PD patients were detected for four SNPs from three genes (serotonin 2A receptor (rs6311, P=0.043), Wolfram syndrome 1 (rs1801211, P=0.007), proopiomelanocortin (rs28930368, P=0.026 and rs2071345, P=0.027) genes).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_provenance.
- NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_assertion evidence source_evidence_literature NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_provenance.
- NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_assertion SIO_000772 16876316 NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_provenance.
- NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_assertion wasDerivedFrom gad-20130706 NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_provenance.
- NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_assertion wasGeneratedBy ECO_0000203 NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_provenance.
- gad-20130706 importedOn "2013-07-06" NP66258.RAJdAiHiRhkxuxwpC7XQn6UpLw15HMT6shRNHyvXWZYWg130_provenance.