Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_provenance.
- NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_assertion description "[Mutations in the gene encoding peroxisomal sterol carrier protein X (SCPx) cause leukencephalopathy with dystonia and motor neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_provenance.
- NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_assertion evidence source_evidence_literature NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_provenance.
- NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_assertion SIO_000772 16685654 NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_provenance.
- NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_assertion wasDerivedFrom befree-20140225 NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_provenance.
- NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_assertion wasGeneratedBy ECO_0000203 NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP818605.RA4mXLAJR8m2ZB5fktcYjf8vNYUtQH6mLFWE7kiTpgZo8130_provenance.