Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_provenance.
- NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_assertion description "[Our results show that genetic variants of the NKG2D receptor are associated with development of CCA in PSC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_provenance.
- NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_assertion evidence source_evidence_literature NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_provenance.
- NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_assertion SIO_000772 18023027 NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_provenance.
- NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_assertion wasDerivedFrom befree-20140225 NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_provenance.
- NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_assertion wasGeneratedBy ECO_0000203 NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP257496.RAQmImrvYcu8VovPcmLh5WVEgsijfuGHjb_6taA3Cu_jE130_provenance.