Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_provenance.
- NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_assertion description "[Mutations in the large GPR98 gene underlie Usher syndrome type 2C (USH2C), and all patients described to date have been female.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_provenance.
- NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_assertion evidence source_evidence_literature NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_provenance.
- NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_assertion SIO_000772 19357117 NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_provenance.
- NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_assertion wasDerivedFrom befree-20140225 NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_provenance.
- NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_assertion wasGeneratedBy ECO_0000203 NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP830060.RAhvBrnyo6LlmED7e1ZPU_IJCcCxrg_L8JJF-5gKIGKAk130_provenance.