Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_provenance.
- NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_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." NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_provenance.
- NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_assertion evidence source_evidence_literature NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_provenance.
- NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_assertion SIO_000772 16700949 NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_provenance.
- NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_assertion wasDerivedFrom befree-2016 NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_provenance.
- NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_assertion wasGeneratedBy ECO_0000203 NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_provenance.
- befree-2016 importedOn "2016-02-19" NP549758.RAJ_VvciTBo_ir2KrH_lTaqBOTHq99U4iTK1cnHGK7AHg130_provenance.