Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP208062.RAqmP5WsMMtxGn_QJ2evB1gmZna9Wrb9Aal1Gtl9kpIWQ130_assertion> ?p ?o ?g. }
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- NP208062.RAqmP5WsMMtxGn_QJ2evB1gmZna9Wrb9Aal1Gtl9kpIWQ130_assertion type Assertion NP208062.RAqmP5WsMMtxGn_QJ2evB1gmZna9Wrb9Aal1Gtl9kpIWQ130_head.
- NP208062.RAqmP5WsMMtxGn_QJ2evB1gmZna9Wrb9Aal1Gtl9kpIWQ130_assertion description "[this defect is a new type of congenital disorder of glycosylation (CDG) of type IIf affecting the transport of CMP-sialic acid into the Golgi apparatus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208062.RAqmP5WsMMtxGn_QJ2evB1gmZna9Wrb9Aal1Gtl9kpIWQ130_provenance.
- NP208062.RAqmP5WsMMtxGn_QJ2evB1gmZna9Wrb9Aal1Gtl9kpIWQ130_assertion evidence source_evidence_literature NP208062.RAqmP5WsMMtxGn_QJ2evB1gmZna9Wrb9Aal1Gtl9kpIWQ130_provenance.
- NP208062.RAqmP5WsMMtxGn_QJ2evB1gmZna9Wrb9Aal1Gtl9kpIWQ130_assertion SIO_000772 15576474 NP208062.RAqmP5WsMMtxGn_QJ2evB1gmZna9Wrb9Aal1Gtl9kpIWQ130_provenance.
- NP208062.RAqmP5WsMMtxGn_QJ2evB1gmZna9Wrb9Aal1Gtl9kpIWQ130_assertion wasDerivedFrom lhgdn-20090331 NP208062.RAqmP5WsMMtxGn_QJ2evB1gmZna9Wrb9Aal1Gtl9kpIWQ130_provenance.
- NP208062.RAqmP5WsMMtxGn_QJ2evB1gmZna9Wrb9Aal1Gtl9kpIWQ130_assertion wasGeneratedBy ECO_0000203 NP208062.RAqmP5WsMMtxGn_QJ2evB1gmZna9Wrb9Aal1Gtl9kpIWQ130_provenance.