Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_provenance.
- NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_assertion description "[This 7-year-old boy with Dejerine-Sottas syndrome caused by a mutation in the myelin protein zero gene began to suffer rapid deterioration with increasing leg weakness, loss of the ability to ambulate, and bowel and bladder incontinence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_provenance.
- NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_assertion evidence source_evidence_literature NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_provenance.
- NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_assertion SIO_000772 12296688 NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_provenance.
- NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_assertion wasDerivedFrom befree-20140225 NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_provenance.
- NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_assertion wasGeneratedBy ECO_0000203 NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP237635.RAWOoL0IVap8dwEsqh3V3L0j8b5ouFykLKAia2XxkiTB8130_provenance.