Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP323224.RAzhS5-np636Y8T_26zcy8t8oHSJMrXdYZQWJXEGIHWZI130_assertion> ?p ?o ?g. }
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- NP323224.RAzhS5-np636Y8T_26zcy8t8oHSJMrXdYZQWJXEGIHWZI130_assertion type Assertion NP323224.RAzhS5-np636Y8T_26zcy8t8oHSJMrXdYZQWJXEGIHWZI130_head.
- NP323224.RAzhS5-np636Y8T_26zcy8t8oHSJMrXdYZQWJXEGIHWZI130_assertion wasGeneratedBy ECO_0000203 NP323224.RAzhS5-np636Y8T_26zcy8t8oHSJMrXdYZQWJXEGIHWZI130_provenance.
- NP323224.RAzhS5-np636Y8T_26zcy8t8oHSJMrXdYZQWJXEGIHWZI130_assertion wasDerivedFrom befree-20140225 NP323224.RAzhS5-np636Y8T_26zcy8t8oHSJMrXdYZQWJXEGIHWZI130_provenance.
- NP323224.RAzhS5-np636Y8T_26zcy8t8oHSJMrXdYZQWJXEGIHWZI130_assertion SIO_000772 10727999 NP323224.RAzhS5-np636Y8T_26zcy8t8oHSJMrXdYZQWJXEGIHWZI130_provenance.
- NP323224.RAzhS5-np636Y8T_26zcy8t8oHSJMrXdYZQWJXEGIHWZI130_assertion evidence source_evidence_literature NP323224.RAzhS5-np636Y8T_26zcy8t8oHSJMrXdYZQWJXEGIHWZI130_provenance.
- NP323224.RAzhS5-np636Y8T_26zcy8t8oHSJMrXdYZQWJXEGIHWZI130_assertion description "[Mutations in the KAL gene (Kallmann syndrome) and the AHC gene (adrenal hypoplasia congenita/HH) cause X-linked recessive HH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323224.RAzhS5-np636Y8T_26zcy8t8oHSJMrXdYZQWJXEGIHWZI130_provenance.