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- source_evidence_literature type ECO_0000212 NP86019.RAGN6AjrmRjPeVnoIGIx5HZ8Q-pL6FojAHfagvN7d86So130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP86019.RAGN6AjrmRjPeVnoIGIx5HZ8Q-pL6FojAHfagvN7d86So130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP86019.RAGN6AjrmRjPeVnoIGIx5HZ8Q-pL6FojAHfagvN7d86So130_provenance.
- NP86019.RAGN6AjrmRjPeVnoIGIx5HZ8Q-pL6FojAHfagvN7d86So130_assertion description "[In conclusion, we present compelling evidence for genetic heterogeneity within Europe. These NOD2/CARD15 variants have a minor contribution in Scottish and Irish CD patients, consistent with an emerging pattern from Northern Europe.Genes and Immunity adva]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86019.RAGN6AjrmRjPeVnoIGIx5HZ8Q-pL6FojAHfagvN7d86So130_provenance.
- NP86019.RAGN6AjrmRjPeVnoIGIx5HZ8Q-pL6FojAHfagvN7d86So130_assertion evidence source_evidence_literature NP86019.RAGN6AjrmRjPeVnoIGIx5HZ8Q-pL6FojAHfagvN7d86So130_provenance.
- NP86019.RAGN6AjrmRjPeVnoIGIx5HZ8Q-pL6FojAHfagvN7d86So130_assertion SIO_000772 15190267 NP86019.RAGN6AjrmRjPeVnoIGIx5HZ8Q-pL6FojAHfagvN7d86So130_provenance.
- NP86019.RAGN6AjrmRjPeVnoIGIx5HZ8Q-pL6FojAHfagvN7d86So130_assertion wasDerivedFrom gad-20150221 NP86019.RAGN6AjrmRjPeVnoIGIx5HZ8Q-pL6FojAHfagvN7d86So130_provenance.
- NP86019.RAGN6AjrmRjPeVnoIGIx5HZ8Q-pL6FojAHfagvN7d86So130_assertion wasGeneratedBy ECO_0000203 NP86019.RAGN6AjrmRjPeVnoIGIx5HZ8Q-pL6FojAHfagvN7d86So130_provenance.
- gad-20150221 importedOn "2015-02-21" NP86019.RAGN6AjrmRjPeVnoIGIx5HZ8Q-pL6FojAHfagvN7d86So130_provenance.