Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_provenance.
- NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_assertion description "[AOA1 is associated with oculomotor apraxia, severe sensorimotor neuropathy, choreiform movements, cognitive impairment, and cerebellar atrophy at an early age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_provenance.
- NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_assertion evidence source_evidence_literature NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_provenance.
- NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_assertion SIO_000772 16700949 NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_provenance.
- NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_assertion wasDerivedFrom befree-20140225 NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_provenance.
- NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_assertion wasGeneratedBy ECO_0000203 NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP752073.RAretc9ETfFAEiVoOJRgjToAnMUzJc1KLWVQEPpIwWpNQ130_provenance.