Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP796833.RA2nuY5CRgZNFbYcHawrKHpfpW977w9eA2zqqIrKYmsuI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP796833.RA2nuY5CRgZNFbYcHawrKHpfpW977w9eA2zqqIrKYmsuI130_assertion type Assertion NP796833.RA2nuY5CRgZNFbYcHawrKHpfpW977w9eA2zqqIrKYmsuI130_head.
- NP796833.RA2nuY5CRgZNFbYcHawrKHpfpW977w9eA2zqqIrKYmsuI130_assertion description "[Mutations in OFD1 also cause X-linked Joubert syndrome (JBTS10) and Simpson-Golabi-Behmel syndrome type 2 (SGBS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796833.RA2nuY5CRgZNFbYcHawrKHpfpW977w9eA2zqqIrKYmsuI130_provenance.
- NP796833.RA2nuY5CRgZNFbYcHawrKHpfpW977w9eA2zqqIrKYmsuI130_assertion evidence source_evidence_literature NP796833.RA2nuY5CRgZNFbYcHawrKHpfpW977w9eA2zqqIrKYmsuI130_provenance.
- NP796833.RA2nuY5CRgZNFbYcHawrKHpfpW977w9eA2zqqIrKYmsuI130_assertion SIO_000772 23033313 NP796833.RA2nuY5CRgZNFbYcHawrKHpfpW977w9eA2zqqIrKYmsuI130_provenance.
- NP796833.RA2nuY5CRgZNFbYcHawrKHpfpW977w9eA2zqqIrKYmsuI130_assertion wasDerivedFrom befree-20150227 NP796833.RA2nuY5CRgZNFbYcHawrKHpfpW977w9eA2zqqIrKYmsuI130_provenance.
- NP796833.RA2nuY5CRgZNFbYcHawrKHpfpW977w9eA2zqqIrKYmsuI130_assertion wasGeneratedBy ECO_0000203 NP796833.RA2nuY5CRgZNFbYcHawrKHpfpW977w9eA2zqqIrKYmsuI130_provenance.