Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_provenance.
- NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_assertion description "[Mucolipidosis type IV (MLIV) is an autosomal recessive, neurodegenerative, lysosomal storage disorder characterized by psychomotor retardation and ophthalmological abnormalities including corneal opacities, retinal degeneration and strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_provenance.
- NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_assertion evidence source_evidence_literature NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_provenance.
- NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_assertion SIO_000772 10973263 NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_provenance.
- NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_assertion wasDerivedFrom befree-20140225 NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_provenance.
- NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_assertion wasGeneratedBy ECO_0000203 NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP204857.RA0mEhTcTY6oZ1qQUYq9YdzcEe2ySLrNZKiR0E-Vh0uLo130_provenance.