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- NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_assertion type Assertion NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_head.
- NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_assertion description "[FBN1 mutations typically cause the Marfan syndrome, an autosomal dominant disorder manifesting with skeletal overgrowth, aortic aneurysm, and lens dislocation (ectopia lentis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance.
- NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_assertion evidence source_evidence_literature NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance.
- NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_assertion SIO_000772 21858451 NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance.
- NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_assertion wasDerivedFrom befree-2016 NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance.
- NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_assertion wasGeneratedBy ECO_0000203 NP918452.RAIouLD7sCvTnHhkl8u2QwM4_oMlM29YcJ4krposTsLu8130_provenance.