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- source_evidence_literature type ECO_0000212 NP434569.RARuwugbfZ9wv8dhySfPrlZOOXGGBVmlaw_Lf2E5LguQ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434569.RARuwugbfZ9wv8dhySfPrlZOOXGGBVmlaw_Lf2E5LguQ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434569.RARuwugbfZ9wv8dhySfPrlZOOXGGBVmlaw_Lf2E5LguQ0130_provenance.
- NP434569.RARuwugbfZ9wv8dhySfPrlZOOXGGBVmlaw_Lf2E5LguQ0130_assertion description "[The distribution of the NR2b genotypes (p = 0.600) and alleles (p = 0.652) did not differ significantly between AD patients and controls, however, suggesting that it is unlikely that the NR2b C2664T polymorphism plays a substantial role in conferring susceptibility to AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434569.RARuwugbfZ9wv8dhySfPrlZOOXGGBVmlaw_Lf2E5LguQ0130_provenance.
- NP434569.RARuwugbfZ9wv8dhySfPrlZOOXGGBVmlaw_Lf2E5LguQ0130_assertion evidence source_evidence_literature NP434569.RARuwugbfZ9wv8dhySfPrlZOOXGGBVmlaw_Lf2E5LguQ0130_provenance.
- NP434569.RARuwugbfZ9wv8dhySfPrlZOOXGGBVmlaw_Lf2E5LguQ0130_assertion SIO_000772 11844890 NP434569.RARuwugbfZ9wv8dhySfPrlZOOXGGBVmlaw_Lf2E5LguQ0130_provenance.
- NP434569.RARuwugbfZ9wv8dhySfPrlZOOXGGBVmlaw_Lf2E5LguQ0130_assertion wasDerivedFrom befree-20150227 NP434569.RARuwugbfZ9wv8dhySfPrlZOOXGGBVmlaw_Lf2E5LguQ0130_provenance.
- NP434569.RARuwugbfZ9wv8dhySfPrlZOOXGGBVmlaw_Lf2E5LguQ0130_assertion wasGeneratedBy ECO_0000203 NP434569.RARuwugbfZ9wv8dhySfPrlZOOXGGBVmlaw_Lf2E5LguQ0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434569.RARuwugbfZ9wv8dhySfPrlZOOXGGBVmlaw_Lf2E5LguQ0130_provenance.