Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_assertion> ?p ?o ?g. }
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- NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_assertion type Assertion NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_head.
- NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_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." NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_provenance.
- NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_assertion evidence source_evidence_literature NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_provenance.
- NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_assertion SIO_000772 10727999 NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_provenance.
- NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_assertion wasDerivedFrom befree-2016 NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_provenance.
- NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_assertion wasGeneratedBy ECO_0000203 NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_provenance.