Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_assertion type Assertion NP662777.RABuaXndi6QBlaT2YQm7KCZfkfxDoOpNQ3PvulfOZKmlE130_head.
- 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.