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- NP231069.RAvI_wKiVUU6qlRVhhGoDLdSupjBbeu2uWIQf9HyDkELM130_assertion type Assertion NP231069.RAvI_wKiVUU6qlRVhhGoDLdSupjBbeu2uWIQf9HyDkELM130_head.
- NP231069.RAvI_wKiVUU6qlRVhhGoDLdSupjBbeu2uWIQf9HyDkELM130_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." NP231069.RAvI_wKiVUU6qlRVhhGoDLdSupjBbeu2uWIQf9HyDkELM130_provenance.
- NP231069.RAvI_wKiVUU6qlRVhhGoDLdSupjBbeu2uWIQf9HyDkELM130_assertion evidence source_evidence_literature NP231069.RAvI_wKiVUU6qlRVhhGoDLdSupjBbeu2uWIQf9HyDkELM130_provenance.
- NP231069.RAvI_wKiVUU6qlRVhhGoDLdSupjBbeu2uWIQf9HyDkELM130_assertion SIO_000772 10727999 NP231069.RAvI_wKiVUU6qlRVhhGoDLdSupjBbeu2uWIQf9HyDkELM130_provenance.
- NP231069.RAvI_wKiVUU6qlRVhhGoDLdSupjBbeu2uWIQf9HyDkELM130_assertion wasDerivedFrom befree-20150227 NP231069.RAvI_wKiVUU6qlRVhhGoDLdSupjBbeu2uWIQf9HyDkELM130_provenance.
- NP231069.RAvI_wKiVUU6qlRVhhGoDLdSupjBbeu2uWIQf9HyDkELM130_assertion wasGeneratedBy ECO_0000203 NP231069.RAvI_wKiVUU6qlRVhhGoDLdSupjBbeu2uWIQf9HyDkELM130_provenance.