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- NP18457.RA8Gx_nNKEl7rzNXj-cSL9cd7PB7l8m--YtjgWnYf_SB0130_assertion type Assertion NP18457.RA8Gx_nNKEl7rzNXj-cSL9cd7PB7l8m--YtjgWnYf_SB0130_head.
- NP18457.RA8Gx_nNKEl7rzNXj-cSL9cd7PB7l8m--YtjgWnYf_SB0130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP18457.RA8Gx_nNKEl7rzNXj-cSL9cd7PB7l8m--YtjgWnYf_SB0130_provenance.
- NP18457.RA8Gx_nNKEl7rzNXj-cSL9cd7PB7l8m--YtjgWnYf_SB0130_assertion evidence source_evidence_curated NP18457.RA8Gx_nNKEl7rzNXj-cSL9cd7PB7l8m--YtjgWnYf_SB0130_provenance.
- NP18457.RA8Gx_nNKEl7rzNXj-cSL9cd7PB7l8m--YtjgWnYf_SB0130_assertion SIO_000772 20493458 NP18457.RA8Gx_nNKEl7rzNXj-cSL9cd7PB7l8m--YtjgWnYf_SB0130_provenance.
- NP18457.RA8Gx_nNKEl7rzNXj-cSL9cd7PB7l8m--YtjgWnYf_SB0130_assertion wasDerivedFrom ctd_human-20150221 NP18457.RA8Gx_nNKEl7rzNXj-cSL9cd7PB7l8m--YtjgWnYf_SB0130_provenance.
- NP18457.RA8Gx_nNKEl7rzNXj-cSL9cd7PB7l8m--YtjgWnYf_SB0130_assertion wasGeneratedBy ECO_0000218 NP18457.RA8Gx_nNKEl7rzNXj-cSL9cd7PB7l8m--YtjgWnYf_SB0130_provenance.