Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_provenance.
- NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_assertion description "[Two brothers with no copy of Cx32, 27 and 25 years old, showed steppage gait, moderate muscle atrophy and weakness, and mild sensory disturbance in the distal parts of the legs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_provenance.
- NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_assertion evidence source_evidence_literature NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_provenance.
- NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_assertion SIO_000772 11266688 NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_provenance.
- NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_assertion wasDerivedFrom befree-20140225 NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_provenance.
- NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_assertion wasGeneratedBy ECO_0000203 NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP870883.RA97II5tKTd4_e2eAHWZzwLAzmX7UtL3oIQI8H9V5PaBY130_provenance.