Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_assertion> ?p ?o ?g. }
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- NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_assertion type Assertion NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_head.
- NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_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." NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_provenance.
- NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_assertion evidence source_evidence_curated NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_provenance.
- NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_assertion SIO_000772 20080860 NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_provenance.
- NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_assertion wasDerivedFrom uniprot-20130724 NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_provenance.
- NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_assertion wasGeneratedBy ECO_0000218 NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_provenance.