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- NP296091.RAMT6ShJT-qXbU_bZkhwuUmAc2dTdPYN18PTwvVtYXoZg130_assertion type Assertion NP296091.RAMT6ShJT-qXbU_bZkhwuUmAc2dTdPYN18PTwvVtYXoZg130_head.
- NP296091.RAMT6ShJT-qXbU_bZkhwuUmAc2dTdPYN18PTwvVtYXoZg130_assertion description "[Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP296091.RAMT6ShJT-qXbU_bZkhwuUmAc2dTdPYN18PTwvVtYXoZg130_provenance.
- NP296091.RAMT6ShJT-qXbU_bZkhwuUmAc2dTdPYN18PTwvVtYXoZg130_assertion evidence source_evidence_literature NP296091.RAMT6ShJT-qXbU_bZkhwuUmAc2dTdPYN18PTwvVtYXoZg130_provenance.
- NP296091.RAMT6ShJT-qXbU_bZkhwuUmAc2dTdPYN18PTwvVtYXoZg130_assertion SIO_000772 20080860 NP296091.RAMT6ShJT-qXbU_bZkhwuUmAc2dTdPYN18PTwvVtYXoZg130_provenance.
- NP296091.RAMT6ShJT-qXbU_bZkhwuUmAc2dTdPYN18PTwvVtYXoZg130_assertion wasDerivedFrom befree-20140225 NP296091.RAMT6ShJT-qXbU_bZkhwuUmAc2dTdPYN18PTwvVtYXoZg130_provenance.
- NP296091.RAMT6ShJT-qXbU_bZkhwuUmAc2dTdPYN18PTwvVtYXoZg130_assertion wasGeneratedBy ECO_0000203 NP296091.RAMT6ShJT-qXbU_bZkhwuUmAc2dTdPYN18PTwvVtYXoZg130_provenance.