Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_provenance.
- NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_assertion description "[Using HHRR and TDT approaches, we found that both polymorphisms were preferentially transmitted to AN offspring (TDT yielded chi(2)=5.01, p=0.025 for NR2B 5073G alleles and chi(2)=11.75, p<0.001 for SK3 L alleles including >19 repeats).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_provenance.
- NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_assertion evidence source_evidence_literature NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_provenance.
- NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_assertion SIO_000772 16157352 NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_provenance.
- NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_assertion wasDerivedFrom befree-20140225 NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_provenance.
- NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_assertion wasGeneratedBy ECO_0000203 NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP725048.RA9tgJxH0DJlETIdWcu91sz8Zyt47_i53tlyg5AT6rY3o130_provenance.