Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_assertion> ?p ?o ?g. }
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- NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_assertion type Assertion NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_head.
- NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_assertion description "[To review three inherited retinal disorders associated with diagnostic or pathognomonic electroretinogram (ERG) abnormalities: cone dystrophy with supernormal rod ERG (KCNV2), enhanced S-cone syndrome (NR2E3), and bradyopsia (RGS9/R9AP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_provenance.
- NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_assertion evidence source_evidence_literature NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_provenance.
- NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_assertion SIO_000772 23263253 NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_provenance.
- NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_assertion wasDerivedFrom befree-20140225 NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_provenance.
- NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_assertion wasGeneratedBy ECO_0000203 NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_provenance.