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- NP1130133.RAY70iZj8jdEnQWIZf-xGxBQcZbFjN01B8-IM8bBzKfqE130_assertion type Assertion NP1130133.RAY70iZj8jdEnQWIZf-xGxBQcZbFjN01B8-IM8bBzKfqE130_head.
- NP1130133.RAY70iZj8jdEnQWIZf-xGxBQcZbFjN01B8-IM8bBzKfqE130_assertion description "[SNP linkage analysis and whole exome sequencing identify a novel POU4F3 mutation in autosomal dominant late-onset nonsyndromic hearing loss (DFNA15).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1130133.RAY70iZj8jdEnQWIZf-xGxBQcZbFjN01B8-IM8bBzKfqE130_provenance.
- NP1130133.RAY70iZj8jdEnQWIZf-xGxBQcZbFjN01B8-IM8bBzKfqE130_assertion evidence source_evidence_literature NP1130133.RAY70iZj8jdEnQWIZf-xGxBQcZbFjN01B8-IM8bBzKfqE130_provenance.
- NP1130133.RAY70iZj8jdEnQWIZf-xGxBQcZbFjN01B8-IM8bBzKfqE130_assertion SIO_000772 24260153 NP1130133.RAY70iZj8jdEnQWIZf-xGxBQcZbFjN01B8-IM8bBzKfqE130_provenance.
- NP1130133.RAY70iZj8jdEnQWIZf-xGxBQcZbFjN01B8-IM8bBzKfqE130_assertion wasDerivedFrom befree-2016 NP1130133.RAY70iZj8jdEnQWIZf-xGxBQcZbFjN01B8-IM8bBzKfqE130_provenance.
- NP1130133.RAY70iZj8jdEnQWIZf-xGxBQcZbFjN01B8-IM8bBzKfqE130_assertion wasGeneratedBy ECO_0000203 NP1130133.RAY70iZj8jdEnQWIZf-xGxBQcZbFjN01B8-IM8bBzKfqE130_provenance.