Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_provenance.
- NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_assertion description "[X-linked congenital stationary night blindness (CSNB) and NYX mutation have not been reported in Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_provenance.
- NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_assertion evidence source_evidence_literature NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_provenance.
- NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_assertion SIO_000772 16670814 NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_provenance.
- NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_assertion wasDerivedFrom befree-20140225 NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_provenance.
- NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_assertion wasGeneratedBy ECO_0000203 NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP653662.RAO7-gUGEykECfenfTMv5vrKe8nCiRwTUrB3BBiyo1m0I130_provenance.