Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_provenance.
- NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_assertion description "[Our purpose was the determination of a possible genotype-phenotype correlation between the copy number of SMN2, NAIP, p44, H4F5 and occludin genes localized in the same SMN1 region (5q13) and the severity of the disease in SMA Tunisian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_provenance.
- NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_assertion evidence source_evidence_literature NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_provenance.
- NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_assertion SIO_000772 21821450 NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_provenance.
- NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_assertion wasDerivedFrom befree-20140225 NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_provenance.
- NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_assertion wasGeneratedBy ECO_0000203 NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP234291.RAv8ql36qCtnG0ATc8G_-l8yTVCA3N59yvH0ZSTGIyRkA130_provenance.