Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_provenance.
- NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_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." NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_provenance.
- NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_assertion evidence source_evidence_literature NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_provenance.
- NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_assertion SIO_000772 11266688 NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_provenance.
- NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_assertion wasDerivedFrom befree-20140225 NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_provenance.
- NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_assertion wasGeneratedBy ECO_0000203 NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP811050.RAcfQNk43VAvCM474_1x2DpSRIHte-LG-cLlO2iROzbPk130_provenance.