Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_provenance.
- NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_assertion description "[The patient presented with exercise-induced paroxysmal gait ataxia and areflexia as an atypical phenotype associated with a novel homozygous DARS2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_provenance.
- NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_assertion evidence source_evidence_literature NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_provenance.
- NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_assertion SIO_000772 21749991 NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_provenance.
- NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_assertion wasDerivedFrom befree-20140225 NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_provenance.
- NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_assertion wasGeneratedBy ECO_0000203 NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP850312.RAumjvQuco_DAe4hLmf3nGg7arI_9sh9P3yof_9oDXOwg130_provenance.