Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_assertion> ?p ?o ?g. }
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- NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_assertion type Assertion NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_head.
- NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_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." NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_provenance.
- NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_assertion evidence source_evidence_literature NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_provenance.
- NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_assertion SIO_000772 17959774 NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_provenance.
- NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_assertion wasDerivedFrom befree-2016 NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_provenance.
- NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_assertion wasGeneratedBy ECO_0000203 NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_provenance.