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- NP2928.RAGfeAVf64-0UogEGuuBNz9AZr4b-r-uGIglFMi_ETryY130_assertion type Assertion NP2928.RAGfeAVf64-0UogEGuuBNz9AZr4b-r-uGIglFMi_ETryY130_head.
- NP2928.RAGfeAVf64-0UogEGuuBNz9AZr4b-r-uGIglFMi_ETryY130_assertion description "[Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2928.RAGfeAVf64-0UogEGuuBNz9AZr4b-r-uGIglFMi_ETryY130_provenance.
- NP2928.RAGfeAVf64-0UogEGuuBNz9AZr4b-r-uGIglFMi_ETryY130_assertion evidence source_evidence_curated NP2928.RAGfeAVf64-0UogEGuuBNz9AZr4b-r-uGIglFMi_ETryY130_provenance.
- NP2928.RAGfeAVf64-0UogEGuuBNz9AZr4b-r-uGIglFMi_ETryY130_assertion SIO_000772 20137778 NP2928.RAGfeAVf64-0UogEGuuBNz9AZr4b-r-uGIglFMi_ETryY130_provenance.
- NP2928.RAGfeAVf64-0UogEGuuBNz9AZr4b-r-uGIglFMi_ETryY130_assertion wasDerivedFrom uniprot-20130724 NP2928.RAGfeAVf64-0UogEGuuBNz9AZr4b-r-uGIglFMi_ETryY130_provenance.
- NP2928.RAGfeAVf64-0UogEGuuBNz9AZr4b-r-uGIglFMi_ETryY130_assertion wasGeneratedBy ECO_0000218 NP2928.RAGfeAVf64-0UogEGuuBNz9AZr4b-r-uGIglFMi_ETryY130_provenance.