Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_assertion> ?p ?o ?g. }
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- NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_assertion type Assertion NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_head.
- NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_assertion description "[High frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21-hydroxylase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_provenance.
- NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_assertion evidence source_evidence_literature NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_provenance.
- NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_assertion SIO_000772 18478071 NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_provenance.
- NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_assertion wasDerivedFrom befree-2016 NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_provenance.
- NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_assertion wasGeneratedBy ECO_0000203 NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_provenance.