Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_provenance.
- NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_assertion description "[40% of all mutations identified among the Polish acute intermittent porphyria (AIP) patients in this study are novel, indicating the heterogeneity of molecular defects causing AIP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_provenance.
- NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_assertion evidence source_evidence_literature NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_provenance.
- NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_assertion SIO_000772 11857754 NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_provenance.
- NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_assertion wasDerivedFrom lhgdn-20090331 NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_provenance.
- NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_assertion wasGeneratedBy ECO_0000203 NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_provenance.