Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP452140.RA0N5p9Do3zUpKIqBOmtwLqkliZDErG7ap7jaCQ1qhMDs130_assertion> ?p ?o ?g. }
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- NP452140.RA0N5p9Do3zUpKIqBOmtwLqkliZDErG7ap7jaCQ1qhMDs130_assertion type Assertion NP452140.RA0N5p9Do3zUpKIqBOmtwLqkliZDErG7ap7jaCQ1qhMDs130_head.
- NP452140.RA0N5p9Do3zUpKIqBOmtwLqkliZDErG7ap7jaCQ1qhMDs130_assertion wasGeneratedBy ECO_0000203 NP452140.RA0N5p9Do3zUpKIqBOmtwLqkliZDErG7ap7jaCQ1qhMDs130_provenance.
- NP452140.RA0N5p9Do3zUpKIqBOmtwLqkliZDErG7ap7jaCQ1qhMDs130_assertion wasDerivedFrom befree-20150227 NP452140.RA0N5p9Do3zUpKIqBOmtwLqkliZDErG7ap7jaCQ1qhMDs130_provenance.
- NP452140.RA0N5p9Do3zUpKIqBOmtwLqkliZDErG7ap7jaCQ1qhMDs130_assertion SIO_000772 6288753 NP452140.RA0N5p9Do3zUpKIqBOmtwLqkliZDErG7ap7jaCQ1qhMDs130_provenance.
- NP452140.RA0N5p9Do3zUpKIqBOmtwLqkliZDErG7ap7jaCQ1qhMDs130_assertion evidence source_evidence_literature NP452140.RA0N5p9Do3zUpKIqBOmtwLqkliZDErG7ap7jaCQ1qhMDs130_provenance.
- NP452140.RA0N5p9Do3zUpKIqBOmtwLqkliZDErG7ap7jaCQ1qhMDs130_assertion description "[The hormonal and genetic linkage studies indicate that the late-onset (symptomatic) form of 21-hydroxylase deficiency, like the cryptic (asymptomatic) and classical forms of 21-hydroxylase deficiency, is transmitted by an autosomal recessive gene which is linked to HLA-B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452140.RA0N5p9Do3zUpKIqBOmtwLqkliZDErG7ap7jaCQ1qhMDs130_provenance.