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- NP357042.RAP-UYcE5ZlGnvoLFE6pUixVjXqUfOdvkHXh5OmkjPDC4130_assertion type Assertion NP357042.RAP-UYcE5ZlGnvoLFE6pUixVjXqUfOdvkHXh5OmkjPDC4130_head.
- NP357042.RAP-UYcE5ZlGnvoLFE6pUixVjXqUfOdvkHXh5OmkjPDC4130_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." NP357042.RAP-UYcE5ZlGnvoLFE6pUixVjXqUfOdvkHXh5OmkjPDC4130_provenance.
- NP357042.RAP-UYcE5ZlGnvoLFE6pUixVjXqUfOdvkHXh5OmkjPDC4130_assertion evidence source_evidence_literature NP357042.RAP-UYcE5ZlGnvoLFE6pUixVjXqUfOdvkHXh5OmkjPDC4130_provenance.
- NP357042.RAP-UYcE5ZlGnvoLFE6pUixVjXqUfOdvkHXh5OmkjPDC4130_assertion SIO_000772 23109149 NP357042.RAP-UYcE5ZlGnvoLFE6pUixVjXqUfOdvkHXh5OmkjPDC4130_provenance.
- NP357042.RAP-UYcE5ZlGnvoLFE6pUixVjXqUfOdvkHXh5OmkjPDC4130_assertion wasDerivedFrom befree-20140225 NP357042.RAP-UYcE5ZlGnvoLFE6pUixVjXqUfOdvkHXh5OmkjPDC4130_provenance.
- NP357042.RAP-UYcE5ZlGnvoLFE6pUixVjXqUfOdvkHXh5OmkjPDC4130_assertion wasGeneratedBy ECO_0000203 NP357042.RAP-UYcE5ZlGnvoLFE6pUixVjXqUfOdvkHXh5OmkjPDC4130_provenance.