Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_provenance.
- NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_assertion description "[The patient carrying the compound heterozygous mutations (R331X and X399R) had attenuated secretion of endogenous gonadotropin-releasing hormone and a left-shifted dose-response curve for gonadotropin-releasing hormone as compared with six patients who had idiopathic hypogonadotropic hypogonadism without GPR54 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_provenance.
- NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_assertion evidence source_evidence_literature NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_provenance.
- NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_assertion SIO_000772 14573733 NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_provenance.
- NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_assertion wasDerivedFrom befree-2016 NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_provenance.
- NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_assertion wasGeneratedBy ECO_0000203 NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_provenance.
- befree-2016 importedOn "2016-02-19" NP417904.RA4S4UaFrjmzTQYXp4vyaMigZN1OG3O79VUNCXYASnoXc130_provenance.