Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_provenance.
- NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_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." NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_provenance.
- NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_assertion evidence source_evidence_literature NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_provenance.
- NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_assertion SIO_000772 16700949 NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_provenance.
- NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_assertion wasDerivedFrom befree-20150227 NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_provenance.
- NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_assertion wasGeneratedBy ECO_0000203 NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914776.RAas2yXJe6dVGJQnme3Z6ZdJ91vePm0LhJ6b1phGc24YI130_provenance.