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- NP523472.RAEhVBp3XrKDqchj7_IPkyB6fFdc29R71JoAOrLiWrjxE130_assertion type Assertion NP523472.RAEhVBp3XrKDqchj7_IPkyB6fFdc29R71JoAOrLiWrjxE130_head.
- NP523472.RAEhVBp3XrKDqchj7_IPkyB6fFdc29R71JoAOrLiWrjxE130_assertion description "[Mutations in 2 of these genes were shown to cause BFNC (KCNQ3) and hereditary deafness (KCNQ4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523472.RAEhVBp3XrKDqchj7_IPkyB6fFdc29R71JoAOrLiWrjxE130_provenance.
- NP523472.RAEhVBp3XrKDqchj7_IPkyB6fFdc29R71JoAOrLiWrjxE130_assertion evidence source_evidence_literature NP523472.RAEhVBp3XrKDqchj7_IPkyB6fFdc29R71JoAOrLiWrjxE130_provenance.
- NP523472.RAEhVBp3XrKDqchj7_IPkyB6fFdc29R71JoAOrLiWrjxE130_assertion SIO_000772 12707061 NP523472.RAEhVBp3XrKDqchj7_IPkyB6fFdc29R71JoAOrLiWrjxE130_provenance.
- NP523472.RAEhVBp3XrKDqchj7_IPkyB6fFdc29R71JoAOrLiWrjxE130_assertion wasDerivedFrom befree-20150227 NP523472.RAEhVBp3XrKDqchj7_IPkyB6fFdc29R71JoAOrLiWrjxE130_provenance.
- NP523472.RAEhVBp3XrKDqchj7_IPkyB6fFdc29R71JoAOrLiWrjxE130_assertion wasGeneratedBy ECO_0000203 NP523472.RAEhVBp3XrKDqchj7_IPkyB6fFdc29R71JoAOrLiWrjxE130_provenance.