Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP418907.RAmUr3hE77tplEf7RAAWj7Ka11WYzYx0r4CZHM8NwMvKk130_provenance.