Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_provenance.
- NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_assertion description "[Mutations in CRB1 are associated with a range of recessively inherited retinal dystrophies, including LCA, childhood- and juvenile-onset rod-cone and cone-rod dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_provenance.
- NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_assertion evidence source_evidence_literature NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_provenance.
- NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_assertion SIO_000772 20956273 NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_provenance.
- NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_assertion wasDerivedFrom befree-20140225 NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_provenance.
- NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_assertion wasGeneratedBy ECO_0000203 NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_provenance.
- befree-20140225 importedOn "2014-02-25" NP444064.RAJ7lr2Rp_boiTYMSkF3BNN_81rTdgemv7OJYLeRxWG74130_provenance.