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- source_evidence_literature type ECO_0000212 NP978108.RAWEFwosr_F71jK939CRm2_KhL5ar2LrurBbVxDCV44oc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978108.RAWEFwosr_F71jK939CRm2_KhL5ar2LrurBbVxDCV44oc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978108.RAWEFwosr_F71jK939CRm2_KhL5ar2LrurBbVxDCV44oc130_provenance.
- NP978108.RAWEFwosr_F71jK939CRm2_KhL5ar2LrurBbVxDCV44oc130_assertion description "[This combination of early infantile spasms followed by a complex movement disorder contributes further to extent the pleiotropy of the ARX-linked 'interneuronopathy' and should lead the clinician to ARX mutation screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978108.RAWEFwosr_F71jK939CRm2_KhL5ar2LrurBbVxDCV44oc130_provenance.
- NP978108.RAWEFwosr_F71jK939CRm2_KhL5ar2LrurBbVxDCV44oc130_assertion evidence source_evidence_literature NP978108.RAWEFwosr_F71jK939CRm2_KhL5ar2LrurBbVxDCV44oc130_provenance.
- NP978108.RAWEFwosr_F71jK939CRm2_KhL5ar2LrurBbVxDCV44oc130_assertion SIO_000772 18468866 NP978108.RAWEFwosr_F71jK939CRm2_KhL5ar2LrurBbVxDCV44oc130_provenance.
- NP978108.RAWEFwosr_F71jK939CRm2_KhL5ar2LrurBbVxDCV44oc130_assertion wasDerivedFrom befree-20150227 NP978108.RAWEFwosr_F71jK939CRm2_KhL5ar2LrurBbVxDCV44oc130_provenance.
- NP978108.RAWEFwosr_F71jK939CRm2_KhL5ar2LrurBbVxDCV44oc130_assertion wasGeneratedBy ECO_0000203 NP978108.RAWEFwosr_F71jK939CRm2_KhL5ar2LrurBbVxDCV44oc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978108.RAWEFwosr_F71jK939CRm2_KhL5ar2LrurBbVxDCV44oc130_provenance.