Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_provenance.
- NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_assertion description "[We conclude that the mutated genotypes of the ScaI polymorphism are negatively associated with overt nephropathy, whereas the mutated genotypes of BstXI polymorphism are positively associated with microalbuminuria. hANP gene variants may exert a protecti]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_provenance.
- NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_assertion evidence source_evidence_literature NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_provenance.
- NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_assertion SIO_000772 11408388 NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_provenance.
- NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_assertion wasDerivedFrom gad-20150221 NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_provenance.
- NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_assertion wasGeneratedBy ECO_0000203 NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_provenance.
- gad-20150221 importedOn "2015-02-21" NP81655.RAa1R2UDY7BzKUxyrZNOVFomJyadDH3LQYu08ZE3I9e2w130_provenance.