Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_provenance.
- NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_assertion description "[Mucopolysaccharidosis type II (MPS II) or Hunter syndrome is a rare lysosomal storage disorder caused by a deficiency of iduronate-2-sulfatase (IDS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_provenance.
- NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_assertion evidence source_evidence_literature NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_provenance.
- NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_assertion SIO_000772 21291454 NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_provenance.
- NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_assertion wasDerivedFrom befree-20150227 NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_provenance.
- NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_assertion wasGeneratedBy ECO_0000203 NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP475518.RArtIaWoIFCZSTrEg9aCoURbjvMIgwj3d85bXA5XnEkfw130_provenance.