Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_assertion> ?p ?o ?g. }
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- NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_assertion type Assertion NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_head.
- NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_assertion description "[Mutations in the SLC26A4 gene (7q22.3-7q31.1) are considered one of the most common causes of genetic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_provenance.
- NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_assertion evidence source_evidence_literature NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_provenance.
- NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_assertion SIO_000772 22717225 NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_provenance.
- NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_assertion wasDerivedFrom befree-2016 NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_provenance.
- NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_assertion wasGeneratedBy ECO_0000203 NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_provenance.