Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_provenance.
- NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_assertion wasGeneratedBy ECO_0000203 NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_provenance.
- NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_assertion wasDerivedFrom befree-20140225 NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_provenance.
- NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_assertion SIO_000772 15370538 NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_provenance.
- NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_assertion evidence source_evidence_literature NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_provenance.
- NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_assertion description "[Leber congenital amaurosis (LCA; estimated prevalence 1 : 50,000-100,000) is an early-onset inherited cause of childhood blindness characterized by a severe retinal dystrophy immediately after birth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP681319.RAVAmBMBOslqVVzsPUFviCIB0W1nXTCzZs-xQ7ob7fxxk130_provenance.