Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_provenance.
- NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_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." NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_provenance.
- NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_assertion evidence source_evidence_literature NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_provenance.
- NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_assertion SIO_000772 19917163 NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_provenance.
- NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_assertion wasDerivedFrom befree-20140225 NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_provenance.
- NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_assertion wasGeneratedBy ECO_0000203 NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP189823.RAPQr0nFY51D4QWi8dWmOT6J9lFZXpXS0sQE1lnxmda7Q130_provenance.