Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_provenance.
- NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_assertion description "[Microsatellite mapping of the deletion in patients with hereditary neuropathy with liability to pressure palsies (HNPP): new molecular tools for the study of the region 17p12 --> p11 and for diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_provenance.
- NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_assertion evidence source_evidence_literature NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_provenance.
- NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_assertion SIO_000772 8565626 NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_provenance.
- NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_assertion wasDerivedFrom befree-20140225 NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_provenance.
- NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_assertion wasGeneratedBy ECO_0000203 NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP790087.RACx13-HJovJPJjvmb5c-LjoHS5ImxS1llZuGLB52WyjU130_provenance.