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- NP606007.RApPvZTvVtWj_lKqHmZjtrvJrL4CmTxmN1EH8cwBD-5ok130_assertion type Assertion NP606007.RApPvZTvVtWj_lKqHmZjtrvJrL4CmTxmN1EH8cwBD-5ok130_head.
- NP606007.RApPvZTvVtWj_lKqHmZjtrvJrL4CmTxmN1EH8cwBD-5ok130_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." NP606007.RApPvZTvVtWj_lKqHmZjtrvJrL4CmTxmN1EH8cwBD-5ok130_provenance.
- NP606007.RApPvZTvVtWj_lKqHmZjtrvJrL4CmTxmN1EH8cwBD-5ok130_assertion evidence source_evidence_literature NP606007.RApPvZTvVtWj_lKqHmZjtrvJrL4CmTxmN1EH8cwBD-5ok130_provenance.
- NP606007.RApPvZTvVtWj_lKqHmZjtrvJrL4CmTxmN1EH8cwBD-5ok130_assertion SIO_000772 10727999 NP606007.RApPvZTvVtWj_lKqHmZjtrvJrL4CmTxmN1EH8cwBD-5ok130_provenance.
- NP606007.RApPvZTvVtWj_lKqHmZjtrvJrL4CmTxmN1EH8cwBD-5ok130_assertion wasDerivedFrom befree-20140225 NP606007.RApPvZTvVtWj_lKqHmZjtrvJrL4CmTxmN1EH8cwBD-5ok130_provenance.
- NP606007.RApPvZTvVtWj_lKqHmZjtrvJrL4CmTxmN1EH8cwBD-5ok130_assertion wasGeneratedBy ECO_0000203 NP606007.RApPvZTvVtWj_lKqHmZjtrvJrL4CmTxmN1EH8cwBD-5ok130_provenance.