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- NP609180.RAs7Q8bjajPW_RZ-JcILFUcafjihHXOar_00oSDx385us130_assertion type Assertion NP609180.RAs7Q8bjajPW_RZ-JcILFUcafjihHXOar_00oSDx385us130_head.
- NP609180.RAs7Q8bjajPW_RZ-JcILFUcafjihHXOar_00oSDx385us130_assertion description "[Infrequently, FBN1 mutations cause dominantly inherited Weill-Marchesani syndrome (WMS), isolated ectopia lentis (IEL), or the fibrotic condition, geleophysic dysplasia (GD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609180.RAs7Q8bjajPW_RZ-JcILFUcafjihHXOar_00oSDx385us130_provenance.
- NP609180.RAs7Q8bjajPW_RZ-JcILFUcafjihHXOar_00oSDx385us130_assertion evidence source_evidence_literature NP609180.RAs7Q8bjajPW_RZ-JcILFUcafjihHXOar_00oSDx385us130_provenance.
- NP609180.RAs7Q8bjajPW_RZ-JcILFUcafjihHXOar_00oSDx385us130_assertion SIO_000772 21858451 NP609180.RAs7Q8bjajPW_RZ-JcILFUcafjihHXOar_00oSDx385us130_provenance.
- NP609180.RAs7Q8bjajPW_RZ-JcILFUcafjihHXOar_00oSDx385us130_assertion wasDerivedFrom befree-20140225 NP609180.RAs7Q8bjajPW_RZ-JcILFUcafjihHXOar_00oSDx385us130_provenance.
- NP609180.RAs7Q8bjajPW_RZ-JcILFUcafjihHXOar_00oSDx385us130_assertion wasGeneratedBy ECO_0000203 NP609180.RAs7Q8bjajPW_RZ-JcILFUcafjihHXOar_00oSDx385us130_provenance.