Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_provenance.
- NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_assertion wasGeneratedBy ECO_0000203 NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_provenance.
- NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_assertion wasDerivedFrom befree-20150227 NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_provenance.
- NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_assertion SIO_000772 17466001 NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_provenance.
- NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_assertion evidence source_evidence_literature NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_provenance.
- NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_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." NP922989.RAqsYnv7uKc_OxuX6DS8ysy5Q54mcaSYj2N6CXJFkm5tg130_provenance.