Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_provenance.
- NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_assertion description "[Detailed analysis of the different PMP22 mutants revealed, in addition to the obvious myelinopathy, distal axonopathy as a characteristic feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_provenance.
- NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_assertion evidence source_evidence_literature NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_provenance.
- NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_assertion SIO_000772 10586249 NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_provenance.
- NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_assertion wasDerivedFrom befree-20140225 NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_provenance.
- NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_assertion wasGeneratedBy ECO_0000203 NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP836134.RArqrOpl_GXenyA3GUulPihMztKNSGd_aGWRwWFtE0cyA130_provenance.