Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_provenance.
- NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_assertion description "[No association was seen with any SNP in LN-PEP, which flanks ERAP1 and was associated with AS in the British population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_provenance.
- NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_assertion evidence source_evidence_literature NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_provenance.
- NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_assertion SIO_000772 19917163 NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_provenance.
- NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_assertion wasDerivedFrom befree-20150227 NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_provenance.
- NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_assertion wasGeneratedBy ECO_0000203 NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP882357.RAQmfG2MYbwX2mtTs4reYRWr4nvln9IVKUNLnOsb6K7wU130_provenance.