Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_provenance.
- NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_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." NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_provenance.
- NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_assertion evidence source_evidence_literature NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_provenance.
- NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_assertion SIO_000772 19732867 NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_provenance.
- NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_assertion wasDerivedFrom befree-20150227 NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_provenance.
- NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_assertion wasGeneratedBy ECO_0000203 NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP968525.RADcJvm5fonsvAJGqz1HELgQM5nSABzJX4pKqmLnnYEAA130_provenance.