Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_provenance.
- NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_assertion description "[Association of a null allele of SPRN with variant Creutzfeldt-Jakob disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_provenance.
- NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_assertion evidence source_evidence_literature NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_provenance.
- NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_assertion SIO_000772 18805828 NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_provenance.
- NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_assertion wasDerivedFrom befree-2016 NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_provenance.
- NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_assertion wasGeneratedBy ECO_0000203 NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_provenance.
- befree-2016 importedOn "2016-02-19" NP694193.RAIi1j6Ld63pU5tHFtYXFZ1rhaAOo3lfwMsTwcVuGmu48130_provenance.