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- NP520838.RAKTTiUuJBGobldDPMtfITzsmcEKFJJhwlogA1u_eCK_c130_assertion type Assertion NP520838.RAKTTiUuJBGobldDPMtfITzsmcEKFJJhwlogA1u_eCK_c130_head.
- NP520838.RAKTTiUuJBGobldDPMtfITzsmcEKFJJhwlogA1u_eCK_c130_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." NP520838.RAKTTiUuJBGobldDPMtfITzsmcEKFJJhwlogA1u_eCK_c130_provenance.
- NP520838.RAKTTiUuJBGobldDPMtfITzsmcEKFJJhwlogA1u_eCK_c130_assertion evidence source_evidence_literature NP520838.RAKTTiUuJBGobldDPMtfITzsmcEKFJJhwlogA1u_eCK_c130_provenance.
- NP520838.RAKTTiUuJBGobldDPMtfITzsmcEKFJJhwlogA1u_eCK_c130_assertion SIO_000772 10727999 NP520838.RAKTTiUuJBGobldDPMtfITzsmcEKFJJhwlogA1u_eCK_c130_provenance.
- NP520838.RAKTTiUuJBGobldDPMtfITzsmcEKFJJhwlogA1u_eCK_c130_assertion wasDerivedFrom befree-20150227 NP520838.RAKTTiUuJBGobldDPMtfITzsmcEKFJJhwlogA1u_eCK_c130_provenance.
- NP520838.RAKTTiUuJBGobldDPMtfITzsmcEKFJJhwlogA1u_eCK_c130_assertion wasGeneratedBy ECO_0000203 NP520838.RAKTTiUuJBGobldDPMtfITzsmcEKFJJhwlogA1u_eCK_c130_provenance.