Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP841038.RAuGikEFhf1tyIhGmk-Ml4Y3zwa3fXoQ7DLGpiJwLhfIE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP841038.RAuGikEFhf1tyIhGmk-Ml4Y3zwa3fXoQ7DLGpiJwLhfIE130_assertion type Assertion NP841038.RAuGikEFhf1tyIhGmk-Ml4Y3zwa3fXoQ7DLGpiJwLhfIE130_head.
- NP841038.RAuGikEFhf1tyIhGmk-Ml4Y3zwa3fXoQ7DLGpiJwLhfIE130_assertion description "[Correct diagnosis of 21-hydroxylase deficiency (21OHD) requires the identification of CYP21A2 gene deletions and CYP21A1P/CYP21A2 chimeric genes, which are disease-causing alleles, and gene duplications, which can lead to false-positive 21OHD allele results.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841038.RAuGikEFhf1tyIhGmk-Ml4Y3zwa3fXoQ7DLGpiJwLhfIE130_provenance.
- NP841038.RAuGikEFhf1tyIhGmk-Ml4Y3zwa3fXoQ7DLGpiJwLhfIE130_assertion evidence source_evidence_literature NP841038.RAuGikEFhf1tyIhGmk-Ml4Y3zwa3fXoQ7DLGpiJwLhfIE130_provenance.
- NP841038.RAuGikEFhf1tyIhGmk-Ml4Y3zwa3fXoQ7DLGpiJwLhfIE130_assertion SIO_000772 17634211 NP841038.RAuGikEFhf1tyIhGmk-Ml4Y3zwa3fXoQ7DLGpiJwLhfIE130_provenance.
- NP841038.RAuGikEFhf1tyIhGmk-Ml4Y3zwa3fXoQ7DLGpiJwLhfIE130_assertion wasDerivedFrom befree-20140225 NP841038.RAuGikEFhf1tyIhGmk-Ml4Y3zwa3fXoQ7DLGpiJwLhfIE130_provenance.
- NP841038.RAuGikEFhf1tyIhGmk-Ml4Y3zwa3fXoQ7DLGpiJwLhfIE130_assertion wasGeneratedBy ECO_0000203 NP841038.RAuGikEFhf1tyIhGmk-Ml4Y3zwa3fXoQ7DLGpiJwLhfIE130_provenance.