Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_provenance.
- NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_assertion wasGeneratedBy ECO_0000203 NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_provenance.
- NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_assertion wasDerivedFrom befree-20150227 NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_provenance.
- NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_assertion SIO_000772 8825055 NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_provenance.
- NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_assertion evidence source_evidence_literature NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_provenance.
- NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_assertion description "[Usher syndrome type I (US1) is an autosomal recessive condition in which three different genes have been already localised (USH1A, USH1B, and USH1C on chromosomes 14q32, 11q13, and 11p15 respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836243.RADfcyaQT66gQ-OTSKa28m-d3hL2FkTVKzat4sNl_vjgc130_provenance.