Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_assertion type Assertion NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_head.
- NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_assertion description "[Homozygous loss-of-function PROK2 mutations cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_provenance.
- NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_assertion evidence source_evidence_literature NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_provenance.
- NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_assertion SIO_000772 17959774 NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_provenance.
- NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_assertion wasDerivedFrom lhgdn-20090331 NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_provenance.
- NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_assertion wasGeneratedBy ECO_0000203 NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_provenance.