Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_provenance.
- NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_assertion description "[This study enables us to estimate the frequency of the SPG3A mutations in France at 39% in families with young-onset autosomal dominant spastic paraplegia after exclusion of SPG4 cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_provenance.
- NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_assertion evidence source_evidence_literature NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_provenance.
- NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_assertion SIO_000772 15596607 NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_provenance.
- NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_assertion wasDerivedFrom befree-20140225 NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_provenance.
- NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_assertion wasGeneratedBy ECO_0000203 NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP699804.RARJ2JvuU34XPiNtPzRVnIt60-hlkd1_QA2E-YvkeeUqA130_provenance.