Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_provenance.
- befree-2016 importedOn "2016-02-19" NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_provenance.
- NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_assertion wasGeneratedBy ECO_0000203 NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_provenance.
- NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_assertion wasDerivedFrom befree-2016 NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_provenance.
- NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_assertion SIO_000772 16060937 NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_provenance.
- NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_assertion evidence source_evidence_literature NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_provenance.
- NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_assertion description "[Choreoacanthocytosis (ChAc) is an autosomal recessive disorder caused by mutations in VPS13A on chromosome 9q21 and characterized by neurodegeneration and red cell acanthocytosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506699.RA4G26jAxIPtJNUdA0yNMZi7H45MW4z3oMBdDZTUUbbUg130_provenance.