Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_provenance.
- NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_assertion description "[Peripheral myelin protein PMP22 deficiency is associated with hereditary neuropathy with liability to pressure palsies (HNPP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_provenance.
- NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_assertion evidence source_evidence_literature NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_provenance.
- NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_assertion SIO_000772 9040737 NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_provenance.
- NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_assertion wasDerivedFrom befree-20140225 NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_provenance.
- NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_assertion wasGeneratedBy ECO_0000203 NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP213318.RAlmq2FNVdRLH1UD4qDbVGaiiuGguZYUda6dbjRNYMTY0130_provenance.