Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_provenance.
- NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_assertion wasGeneratedBy ECO_0000203 NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_provenance.
- NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_assertion wasDerivedFrom befree-20140225 NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_provenance.
- NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_assertion SIO_000772 21545237 NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_provenance.
- NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_assertion evidence source_evidence_literature NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_provenance.
- NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_assertion description "[We report a novel G61R SOD1 mutation in a patient with a distinct phenotype including prominent lower motor neuron dysfunction, proximal weakness and atrophy with asymmetrical onset in the thigh and buttock and relentless clinical course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP716502.RAnlFaOCcASVyCYr-rYoXtO9QF4l0UqgUU_jpT2XyCWbw130_provenance.