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- source_evidence_literature type ECO_0000212 NP1293043.RApjdqwG_ZshgBLqDoU_YI6NxDtWbzAVHk217uhN937oA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293043.RApjdqwG_ZshgBLqDoU_YI6NxDtWbzAVHk217uhN937oA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293043.RApjdqwG_ZshgBLqDoU_YI6NxDtWbzAVHk217uhN937oA130_provenance.
- NP1293043.RApjdqwG_ZshgBLqDoU_YI6NxDtWbzAVHk217uhN937oA130_assertion description "[The GUCY2D mutations were found in 47% of the patients (7/15) with autosomal dominant cone dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293043.RApjdqwG_ZshgBLqDoU_YI6NxDtWbzAVHk217uhN937oA130_provenance.
- NP1293043.RApjdqwG_ZshgBLqDoU_YI6NxDtWbzAVHk217uhN937oA130_assertion evidence source_evidence_literature NP1293043.RApjdqwG_ZshgBLqDoU_YI6NxDtWbzAVHk217uhN937oA130_provenance.
- NP1293043.RApjdqwG_ZshgBLqDoU_YI6NxDtWbzAVHk217uhN937oA130_assertion SIO_000772 26298565 NP1293043.RApjdqwG_ZshgBLqDoU_YI6NxDtWbzAVHk217uhN937oA130_provenance.
- NP1293043.RApjdqwG_ZshgBLqDoU_YI6NxDtWbzAVHk217uhN937oA130_assertion wasDerivedFrom befree-2016 NP1293043.RApjdqwG_ZshgBLqDoU_YI6NxDtWbzAVHk217uhN937oA130_provenance.
- NP1293043.RApjdqwG_ZshgBLqDoU_YI6NxDtWbzAVHk217uhN937oA130_assertion wasGeneratedBy ECO_0000203 NP1293043.RApjdqwG_ZshgBLqDoU_YI6NxDtWbzAVHk217uhN937oA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293043.RApjdqwG_ZshgBLqDoU_YI6NxDtWbzAVHk217uhN937oA130_provenance.