Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_provenance.
- NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_assertion wasGeneratedBy ECO_0000203 NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_provenance.
- NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_assertion wasDerivedFrom befree-20140225 NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_provenance.
- NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_assertion SIO_000772 17466001 NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_provenance.
- NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_assertion evidence source_evidence_literature NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_provenance.
- NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_assertion description "[Patients lacked mutations in other genes known to cause ACTH resistance, including AAAS for patients diagnosed with triple A syndrome and MC2R and MRAP for patients diagnosed with familial glucocorticoid deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP470372.RAkyeJxUQm_8qh5MimtKlP8KyodfzsIr05Kb1b7UqT3aE130_provenance.