Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_provenance.
- NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_assertion wasGeneratedBy ECO_0000218 NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_provenance.
- NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_assertion wasDerivedFrom uniprot-20130724 NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_provenance.
- NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_assertion SIO_000772 12050206 NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_provenance.
- NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_assertion evidence source_evidence_curated NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_provenance.
- NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_assertion description "[Mutant luteinizing hormone receptors in a compound heterozygous patient with complete Leydig cell hypoplasia: abnormal processing causes signaling deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP3773.RAYYV_YLRsWJfedcEO74_oCRwmLvwxDqur8-CS8ATPqEQ130_provenance.