Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP278610.RA6u5SuRuXvnGmwk7IOzdlP3S9ktS5qUAyRuiM16Lae_A130_provenance.