Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP936083.RAoYptj-p6dIjZSubBLygCkADFyIorcqH2E012k71UvJ0130_assertion> ?p ?o ?g. }
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- NP936083.RAoYptj-p6dIjZSubBLygCkADFyIorcqH2E012k71UvJ0130_assertion type Assertion NP936083.RAoYptj-p6dIjZSubBLygCkADFyIorcqH2E012k71UvJ0130_head.
- NP936083.RAoYptj-p6dIjZSubBLygCkADFyIorcqH2E012k71UvJ0130_assertion description "[Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936083.RAoYptj-p6dIjZSubBLygCkADFyIorcqH2E012k71UvJ0130_provenance.
- NP936083.RAoYptj-p6dIjZSubBLygCkADFyIorcqH2E012k71UvJ0130_assertion evidence source_evidence_literature NP936083.RAoYptj-p6dIjZSubBLygCkADFyIorcqH2E012k71UvJ0130_provenance.
- NP936083.RAoYptj-p6dIjZSubBLygCkADFyIorcqH2E012k71UvJ0130_assertion SIO_000772 17959774 NP936083.RAoYptj-p6dIjZSubBLygCkADFyIorcqH2E012k71UvJ0130_provenance.
- NP936083.RAoYptj-p6dIjZSubBLygCkADFyIorcqH2E012k71UvJ0130_assertion wasDerivedFrom befree-20150227 NP936083.RAoYptj-p6dIjZSubBLygCkADFyIorcqH2E012k71UvJ0130_provenance.
- NP936083.RAoYptj-p6dIjZSubBLygCkADFyIorcqH2E012k71UvJ0130_assertion wasGeneratedBy ECO_0000203 NP936083.RAoYptj-p6dIjZSubBLygCkADFyIorcqH2E012k71UvJ0130_provenance.