Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_assertion> ?p ?o ?g. }
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- NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_assertion type Assertion NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_head.
- NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_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." NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance.
- NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_assertion evidence source_evidence_literature NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance.
- NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_assertion SIO_000772 17959774 NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance.
- NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_assertion wasDerivedFrom lhgdn-20090331 NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance.
- NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_assertion wasGeneratedBy ECO_0000203 NP210150.RAWnfv89SxyMH2rYyTpje7WgGkfNt0qBzNbtqt6XudFBc130_provenance.