Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP663175.RAhqOs56Ff7I1Dof-QEbhGwXCAjyXBvg-yiZ073xGHT9o130_provenance.