Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_provenance.
- NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_assertion description "[Allan-Herndon-Dudley syndrome (AHDS) caused by a novel SLC16A2 gene mutation showing severe neurologic features and unexpectedly low TRH-stimulated serum TSH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_provenance.
- NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_assertion evidence source_evidence_literature NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_provenance.
- NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_assertion SIO_000772 20713192 NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_provenance.
- NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_assertion wasDerivedFrom befree-20150227 NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_provenance.
- NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_assertion wasGeneratedBy ECO_0000203 NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_provenance.
- befree-20150227 importedOn "2015-02-27" NP700756.RACRa0_e26VFyCgcKajdy2OI1Mx_3YW-ueGin8z3N-Dho130_provenance.