Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_assertion> ?p ?o ?g. }
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- NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_assertion type Assertion NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_head.
- NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_assertion description "[Mutations of the gap junction beta 2 (GJB2) gene coding for the protein connexin 26 account for up to 50% of nonsyndromic sensorineural hearing loss (NSHL), with specific mutations associated with distinct ethnic groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_provenance.
- NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_assertion evidence source_evidence_literature NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_provenance.
- NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_assertion SIO_000772 12169891 NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_provenance.
- NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_assertion wasDerivedFrom befree-20140225 NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_provenance.
- NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_assertion wasGeneratedBy ECO_0000203 NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_provenance.