Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_provenance.
- NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_assertion description "[This patient is the first case of sporadic CJD with plaque-forming MM1-type PrP, suggesting either a shared prion strain with the plaque-forming subset of dural graft-associated CJD or shared host genetic factors that are unrelated to the PrP genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_provenance.
- NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_assertion evidence source_evidence_literature NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_provenance.
- NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_assertion SIO_000772 12578942 NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_provenance.
- NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_assertion wasDerivedFrom befree-2016 NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_provenance.
- NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_assertion wasGeneratedBy ECO_0000203 NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_provenance.
- befree-2016 importedOn "2016-02-19" NP383363.RA3Qk7HsdyPy8RlR-CXo1qekHT6IWTSpqw6fQfBm2wSys130_provenance.