Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_assertion type Assertion NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_head.
- NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_assertion description "[deficiency causes a new congenital disorder of glycosylation (CDG), designated type IId (CDG-IId), a severe neurologic disease characterized by hydrocephalus, myopathy, and blood-clotting defects ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_provenance.
- NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_assertion evidence source_evidence_literature NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_provenance.
- NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_assertion SIO_000772 11901181 NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_provenance.
- NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_assertion wasDerivedFrom lhgdn-20090331 NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_provenance.
- NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_assertion wasGeneratedBy ECO_0000203 NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_provenance.