Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_provenance.
- NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_assertion description "[Our data suggests that epilepsy may be a rare associated feature in children with muscular dystrophy secondary to dystrophin deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_provenance.
- NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_assertion evidence source_evidence_literature NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_provenance.
- NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_assertion SIO_000772 10728205 NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_provenance.
- NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_assertion wasDerivedFrom befree-20140225 NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_provenance.
- NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_assertion wasGeneratedBy ECO_0000203 NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP500120.RAWHcXBIj9l1O2UAEZWAOIEvJ88tdf8npapgrmGPRCmoI130_provenance.