Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_assertion type Assertion NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_head.
- NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_assertion wasGeneratedBy ECO_0000218 NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_provenance.
- NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_assertion wasDerivedFrom ctd_human-2016 NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_provenance.
- NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_assertion SIO_000772 20493458 NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_provenance.
- NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_assertion evidence source_evidence_curated NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_provenance.
- NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_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." NP26213.RArY-cUxu_cO5IefnrzOF4AEARgRl6JUidgqQ4RQaSPi4130_provenance.