Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_provenance.
- befree-2016 importedOn "2016-02-19" NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_provenance.
- NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_assertion wasGeneratedBy ECO_0000203 NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_provenance.
- NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_assertion wasDerivedFrom befree-2016 NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_provenance.
- NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_assertion SIO_000772 15351017 NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_provenance.
- NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_assertion evidence source_evidence_literature NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_provenance.
- NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_assertion description "[In this group, protein-O-linked mannose-beta1,2-N-acetylglucosaminyltransferase and protein-O-mannosyltransferase 1 are considered to be responsible for muscle-eye-brain disease and Walker-Warburg syndrome, respectively, by glycosylation of alpha-dystroglycan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP458777.RAqra1n8G_w7kx6qJMMPb7G1vP3haCv3jv6rIR2Jo9OmM130_provenance.