Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_provenance.
- NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_assertion description "[Based on the studies in mice, we screened DNA from human families segregating deafness and identified a mutation in LOXHD1, which causes DFNB77, a progressive form of autosomal-recessive nonsyndromic hearing loss (ARNSHL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_provenance.
- NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_assertion evidence source_evidence_literature NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_provenance.
- NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_assertion SIO_000772 19732867 NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_provenance.
- NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_assertion wasDerivedFrom befree-20140225 NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_provenance.
- NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_assertion wasGeneratedBy ECO_0000203 NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_provenance.