Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_provenance.
- NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_assertion description "[The PRNP variant allele Asn171Ser is associated with epileptogenesis and highly prevalent in patients with medically untreatable mesial temporal sclerosis with hippocampal sclerosis and influences their surgical outcome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_provenance.
- NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_assertion evidence source_evidence_literature NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_provenance.
- NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_assertion SIO_000772 14610121 NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_provenance.
- NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_assertion wasDerivedFrom lhgdn-20090331 NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_provenance.
- NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_assertion wasGeneratedBy ECO_0000203 NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP196659.RAqrGo-Slc0F8g1ZtBO-_YSLcmr6VJi0AzywnMP_UnmRE130_provenance.