Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP938875.RAEjZZYreQJ4vIz2QNs_l2lgBkuiUhEZVqRWh4Q_Eb4CE130_assertion> ?p ?o ?g. }
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- NP938875.RAEjZZYreQJ4vIz2QNs_l2lgBkuiUhEZVqRWh4Q_Eb4CE130_assertion type Assertion NP938875.RAEjZZYreQJ4vIz2QNs_l2lgBkuiUhEZVqRWh4Q_Eb4CE130_head.
- NP938875.RAEjZZYreQJ4vIz2QNs_l2lgBkuiUhEZVqRWh4Q_Eb4CE130_assertion description "[Hence, mutations have now been described in the genes for the 3 subunits of DPM: DPM1, DPM2, and DPM3, whereby DPM2-CDG links the congenital disorders of glycosylation to the congenital muscular dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938875.RAEjZZYreQJ4vIz2QNs_l2lgBkuiUhEZVqRWh4Q_Eb4CE130_provenance.
- NP938875.RAEjZZYreQJ4vIz2QNs_l2lgBkuiUhEZVqRWh4Q_Eb4CE130_assertion evidence source_evidence_literature NP938875.RAEjZZYreQJ4vIz2QNs_l2lgBkuiUhEZVqRWh4Q_Eb4CE130_provenance.
- NP938875.RAEjZZYreQJ4vIz2QNs_l2lgBkuiUhEZVqRWh4Q_Eb4CE130_assertion SIO_000772 23109149 NP938875.RAEjZZYreQJ4vIz2QNs_l2lgBkuiUhEZVqRWh4Q_Eb4CE130_provenance.
- NP938875.RAEjZZYreQJ4vIz2QNs_l2lgBkuiUhEZVqRWh4Q_Eb4CE130_assertion wasDerivedFrom befree-20140225 NP938875.RAEjZZYreQJ4vIz2QNs_l2lgBkuiUhEZVqRWh4Q_Eb4CE130_provenance.
- NP938875.RAEjZZYreQJ4vIz2QNs_l2lgBkuiUhEZVqRWh4Q_Eb4CE130_assertion wasGeneratedBy ECO_0000203 NP938875.RAEjZZYreQJ4vIz2QNs_l2lgBkuiUhEZVqRWh4Q_Eb4CE130_provenance.