Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_provenance.
- befree-2016 importedOn "2016-02-19" NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_provenance.
- NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_assertion wasGeneratedBy ECO_0000203 NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_provenance.
- NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_assertion wasDerivedFrom befree-2016 NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_provenance.
- NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_assertion SIO_000772 19804849 NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_provenance.
- NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_assertion evidence source_evidence_literature NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_provenance.
- NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_assertion description "[This assay displays 100% specificity and 100% sensitivity for detecting FMR1 methylation, successfully distinguishing normal males from males with full-mutation FXS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767396.RAzzV7_rl82YrKp-lUHq_SfwgiJL6zLMnNsZ1HB_5B4VM130_provenance.