Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_provenance.
- NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_assertion description "[This case appears to be unique in respect to the underlying novel mutation in the ABC1 gene and its association with complete endoneurial sclerosis of all fascicles in the sural nerve and absence of cardiovascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_provenance.
- NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_assertion evidence source_evidence_literature NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_provenance.
- NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_assertion SIO_000772 12615648 NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_provenance.
- NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_assertion wasDerivedFrom befree-20140225 NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_provenance.
- NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_assertion wasGeneratedBy ECO_0000203 NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP467579.RAZaILZ20THV6_71hkl4Ko8xn-fHwr1Tq3JlNVKpd47c4130_provenance.