Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance.
- NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_assertion description "[The aim of our study was to identify point mutations in a group of 606 patients diagnosed for spinal muscular atrophy with excluded biallelic loss of the SMN1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance.
- NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_assertion evidence source_evidence_literature NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance.
- NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_assertion SIO_000772 24844453 NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance.
- NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_assertion wasDerivedFrom befree-2016 NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance.
- NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_assertion wasGeneratedBy ECO_0000203 NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance.