Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_provenance.
- NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_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." NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_provenance.
- NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_assertion evidence source_evidence_literature NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_provenance.
- NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_assertion SIO_000772 21821450 NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_provenance.
- NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_assertion wasDerivedFrom befree-20140225 NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_provenance.
- NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_assertion wasGeneratedBy ECO_0000203 NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_provenance.