Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP198142.RAaft31JZJah9E-7tOSXQXQ-C8H2Vq0mzdtQ8Ng4WQiDk130_provenance.