Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_provenance.
- NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_assertion description "[In the current study, we report the identification of a novel disease-causing mutation in the ASAH1 gene that results in Farber disease in an Indian family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_provenance.
- NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_assertion evidence source_evidence_literature NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_provenance.
- NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_assertion SIO_000772 16951918 NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_provenance.
- NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_assertion wasDerivedFrom befree-2016 NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_provenance.
- NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_assertion wasGeneratedBy ECO_0000203 NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_provenance.
- befree-2016 importedOn "2016-02-19" NP567638.RAF8XVIWK0GiCxZdqX9xeMXG-Sb9GckkDl2JlglGC5fVc130_provenance.