Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_provenance.
- NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_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." NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_provenance.
- NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_assertion evidence source_evidence_literature NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_provenance.
- NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_assertion SIO_000772 15576474 NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_provenance.
- NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_assertion wasDerivedFrom lhgdn-20090331 NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_provenance.
- NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_assertion wasGeneratedBy ECO_0000203 NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP122374.RARsFjrpr29e98V5BOfxRbH3yL62jVIU0_YyixneCysqQ130_provenance.