Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance.
- NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_assertion description "[Of the 83 patients, 61 (73%) possessed the DR4 allele and within this group we have investigated the relative frequencies of two DQ beta gene variants of DQw3, DQw7 and DQw8, one of which we had previously found to be raised in Felty's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance.
- NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_assertion evidence source_evidence_literature NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance.
- NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_assertion SIO_000772 2571385 NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance.
- NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_assertion wasDerivedFrom befree-20140225 NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance.
- NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_assertion wasGeneratedBy ECO_0000203 NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance.