Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_provenance.
- NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_assertion description "[A deleterious mutation in the LOXHD1 gene causes autosomal recessive hearing loss in Ashkenazi Jews.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_provenance.
- NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_assertion evidence source_evidence_literature NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_provenance.
- NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_assertion SIO_000772 21465660 NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_provenance.
- NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_assertion wasDerivedFrom befree-20140225 NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_provenance.
- NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_assertion wasGeneratedBy ECO_0000203 NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615755.RAEL4eAMErzAipC0sZ2gcxd1Wj7CJ-LR7VCHBHPHXwr9A130_provenance.