Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_provenance.
- NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_assertion description "[An incidence of approximately 1 in 107,000 live births was obtained for MPS IH (Hurler phenotype); 1 in 320,000 live births (1 in 165,000 male live births) for MPS II (Hunter Syndrome); 1 in 58,000 for MPS III (Sanfilippo Syndrome); 1 in 640,000 for MPS IVA (Morquio Syndrome type A), and 1 in 320,000 for MPS VI (Maroteaux-Lamy Syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_provenance.
- NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_assertion evidence source_evidence_literature NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_provenance.
- NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_assertion SIO_000772 14608657 NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_provenance.
- NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_assertion wasDerivedFrom befree-20150227 NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_provenance.
- NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_assertion wasGeneratedBy ECO_0000203 NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP475546.RAZwcKHbchqxl6Wf2YJUSQCGT-9_lL6ydbcHb0Y4KoOVo130_provenance.