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- source_evidence_literature type ECO_0000212 NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_provenance.
- NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_provenance.
- NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_assertion evidence source_evidence_literature NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_provenance.
- NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_assertion SIO_000772 12687499 NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_provenance.
- NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_assertion wasDerivedFrom befree-20150227 NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_provenance.
- NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_assertion wasGeneratedBy ECO_0000203 NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_provenance.