Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_provenance.
- NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_assertion wasGeneratedBy ECO_0000218 NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_provenance.
- NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_assertion wasDerivedFrom ctd_human-2016 NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_provenance.
- NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_assertion SIO_000772 11146471 NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_provenance.
- NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_assertion evidence source_evidence_curated NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_provenance.
- NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_assertion description "[Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11094.RAD2e-u5WVzGrTMwRqrGB-uMu7obFmJd5K_kTnwmZZzSo130_provenance.