Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_provenance.
- NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_assertion description "[The polymerase chain reaction was used to screen DNA samples from 12 unrelated individuals with various familial dementias and ataxias for mutation in part of the prion protein (PrP) gene, an abnormality that occurs in individuals with the spongiform encephalopathies, Gerstmann-Str�ussler syndrome (GSS) and Creutzfeldt-Jakob disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_provenance.
- NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_assertion evidence source_evidence_literature NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_provenance.
- NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_assertion SIO_000772 2567794 NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_provenance.
- NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_assertion wasDerivedFrom befree-2016 NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_provenance.
- NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_assertion wasGeneratedBy ECO_0000203 NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1263388.RAuJzoZQivd0WsOnucC06dd1qFtJcLJFWzDZ4Qnf-2B2U130_provenance.