Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP319078.RAfFBZ62nt5BlYP-QERv-15ewbZsUd0pww6PAjC_tQUQo130_assertion> ?p ?o ?g. }
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- NP319078.RAfFBZ62nt5BlYP-QERv-15ewbZsUd0pww6PAjC_tQUQo130_assertion type Assertion NP319078.RAfFBZ62nt5BlYP-QERv-15ewbZsUd0pww6PAjC_tQUQo130_head.
- NP319078.RAfFBZ62nt5BlYP-QERv-15ewbZsUd0pww6PAjC_tQUQo130_assertion wasGeneratedBy ECO_0000203 NP319078.RAfFBZ62nt5BlYP-QERv-15ewbZsUd0pww6PAjC_tQUQo130_provenance.
- NP319078.RAfFBZ62nt5BlYP-QERv-15ewbZsUd0pww6PAjC_tQUQo130_assertion wasDerivedFrom befree-20140225 NP319078.RAfFBZ62nt5BlYP-QERv-15ewbZsUd0pww6PAjC_tQUQo130_provenance.
- NP319078.RAfFBZ62nt5BlYP-QERv-15ewbZsUd0pww6PAjC_tQUQo130_assertion SIO_000772 10412368 NP319078.RAfFBZ62nt5BlYP-QERv-15ewbZsUd0pww6PAjC_tQUQo130_provenance.
- NP319078.RAfFBZ62nt5BlYP-QERv-15ewbZsUd0pww6PAjC_tQUQo130_assertion evidence source_evidence_literature NP319078.RAfFBZ62nt5BlYP-QERv-15ewbZsUd0pww6PAjC_tQUQo130_provenance.
- NP319078.RAfFBZ62nt5BlYP-QERv-15ewbZsUd0pww6PAjC_tQUQo130_assertion description "[Absence of DAX-1 is responsible for adrenal hypoplasia congenita, a human inherited disorder characterized by adrenal insufficiency and hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319078.RAfFBZ62nt5BlYP-QERv-15ewbZsUd0pww6PAjC_tQUQo130_provenance.