Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_provenance.
- NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_assertion description "[Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_provenance.
- NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_assertion evidence source_evidence_literature NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_provenance.
- NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_assertion SIO_000772 19732867 NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_provenance.
- NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_assertion wasDerivedFrom befree-2016 NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_provenance.
- NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_assertion wasGeneratedBy ECO_0000203 NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_provenance.
- befree-2016 importedOn "2016-02-19" NP761452.RAU_ywoPHsgQsIU6NeqhRyN6krS7Vup5VXep9xYJdbNbM130_provenance.