Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_provenance.
- NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_assertion description "[Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_provenance.
- NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_assertion evidence source_evidence_literature NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_provenance.
- NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_assertion SIO_000772 21821450 NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_provenance.
- NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_assertion wasDerivedFrom befree-20150227 NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_provenance.
- NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_assertion wasGeneratedBy ECO_0000203 NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP793995.RAqTzHRylCUi5aiFDRRFtUZC9YUanD_NnZuKZ75B7FWyk130_provenance.