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- NP294884.RAaDQqkfej9sW4-8afPpKXr7SQ1l7HjWH5u-g7eq2gcF0130_assertion type Assertion NP294884.RAaDQqkfej9sW4-8afPpKXr7SQ1l7HjWH5u-g7eq2gcF0130_head.
- NP294884.RAaDQqkfej9sW4-8afPpKXr7SQ1l7HjWH5u-g7eq2gcF0130_assertion description "[Mutations in the GJB2 gene are a major cause of autosomal recessive and sporadic types of congenital deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294884.RAaDQqkfej9sW4-8afPpKXr7SQ1l7HjWH5u-g7eq2gcF0130_provenance.
- NP294884.RAaDQqkfej9sW4-8afPpKXr7SQ1l7HjWH5u-g7eq2gcF0130_assertion evidence source_evidence_literature NP294884.RAaDQqkfej9sW4-8afPpKXr7SQ1l7HjWH5u-g7eq2gcF0130_provenance.
- NP294884.RAaDQqkfej9sW4-8afPpKXr7SQ1l7HjWH5u-g7eq2gcF0130_assertion SIO_000772 10983956 NP294884.RAaDQqkfej9sW4-8afPpKXr7SQ1l7HjWH5u-g7eq2gcF0130_provenance.
- NP294884.RAaDQqkfej9sW4-8afPpKXr7SQ1l7HjWH5u-g7eq2gcF0130_assertion wasDerivedFrom befree-2016 NP294884.RAaDQqkfej9sW4-8afPpKXr7SQ1l7HjWH5u-g7eq2gcF0130_provenance.
- NP294884.RAaDQqkfej9sW4-8afPpKXr7SQ1l7HjWH5u-g7eq2gcF0130_assertion wasGeneratedBy ECO_0000203 NP294884.RAaDQqkfej9sW4-8afPpKXr7SQ1l7HjWH5u-g7eq2gcF0130_provenance.