Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP620244.RA-vx9cClTxp0rD_X9X0XDxtGRiDp0Zw603vVnvo0VO6c130_assertion> ?p ?o ?g. }
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- NP620244.RA-vx9cClTxp0rD_X9X0XDxtGRiDp0Zw603vVnvo0VO6c130_assertion type Assertion NP620244.RA-vx9cClTxp0rD_X9X0XDxtGRiDp0Zw603vVnvo0VO6c130_head.
- NP620244.RA-vx9cClTxp0rD_X9X0XDxtGRiDp0Zw603vVnvo0VO6c130_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." NP620244.RA-vx9cClTxp0rD_X9X0XDxtGRiDp0Zw603vVnvo0VO6c130_provenance.
- NP620244.RA-vx9cClTxp0rD_X9X0XDxtGRiDp0Zw603vVnvo0VO6c130_assertion evidence source_evidence_literature NP620244.RA-vx9cClTxp0rD_X9X0XDxtGRiDp0Zw603vVnvo0VO6c130_provenance.
- NP620244.RA-vx9cClTxp0rD_X9X0XDxtGRiDp0Zw603vVnvo0VO6c130_assertion SIO_000772 10727999 NP620244.RA-vx9cClTxp0rD_X9X0XDxtGRiDp0Zw603vVnvo0VO6c130_provenance.
- NP620244.RA-vx9cClTxp0rD_X9X0XDxtGRiDp0Zw603vVnvo0VO6c130_assertion wasDerivedFrom befree-20150227 NP620244.RA-vx9cClTxp0rD_X9X0XDxtGRiDp0Zw603vVnvo0VO6c130_provenance.
- NP620244.RA-vx9cClTxp0rD_X9X0XDxtGRiDp0Zw603vVnvo0VO6c130_assertion wasGeneratedBy ECO_0000203 NP620244.RA-vx9cClTxp0rD_X9X0XDxtGRiDp0Zw603vVnvo0VO6c130_provenance.