Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_provenance.
- NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_assertion description "[The common prion protein gene (PRNP) codon 129 polymorphism is a strong susceptibility factor for human prion diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_provenance.
- NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_assertion evidence source_evidence_literature NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_provenance.
- NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_assertion SIO_000772 18191917 NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_provenance.
- NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_assertion wasDerivedFrom gad-20130706 NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_provenance.
- NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_assertion wasGeneratedBy ECO_0000203 NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_provenance.
- gad-20130706 importedOn "2013-07-06" NP52699.RAf5BZ-pD5EExktpRVERCchuI2lqOc2P3-QbhrS_uwiJE130_provenance.