Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_provenance.
- NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_assertion wasGeneratedBy ECO_0000203 NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_provenance.
- NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_assertion wasDerivedFrom befree-20150227 NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_provenance.
- NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_assertion SIO_000772 21899441 NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_provenance.
- NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_assertion evidence source_evidence_literature NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_provenance.
- NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_assertion description "[The congenital disorder of glycosylation (CDG)-Ic (ALG6-CDG, CDG-Ic) is caused by mutations in the hALG6 gene that encodes the N-glycosylation pathway enzyme, α-1,3-glucosyltransferase (NP_037471.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP894936.RABAk89PHpXUXsIThpnE9m0ylsxO3fdtZfNkcjRZJrpvE130_provenance.