Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_assertion> ?p ?o ?g. }
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- NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_assertion type Assertion NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_head.
- NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_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." NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_provenance.
- NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_assertion evidence source_evidence_literature NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_provenance.
- NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_assertion SIO_000772 10727999 NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_provenance.
- NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_assertion wasDerivedFrom befree-20140225 NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_provenance.
- NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_assertion wasGeneratedBy ECO_0000203 NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_provenance.