Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP762351.RAm-E22mgRJsiTfoy_iVmSVF5f-Tw3W96jpkz2Hnuc62Q130_assertion> ?p ?o ?g. }
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- NP762351.RAm-E22mgRJsiTfoy_iVmSVF5f-Tw3W96jpkz2Hnuc62Q130_assertion type Assertion NP762351.RAm-E22mgRJsiTfoy_iVmSVF5f-Tw3W96jpkz2Hnuc62Q130_head.
- NP762351.RAm-E22mgRJsiTfoy_iVmSVF5f-Tw3W96jpkz2Hnuc62Q130_assertion wasGeneratedBy ECO_0000203 NP762351.RAm-E22mgRJsiTfoy_iVmSVF5f-Tw3W96jpkz2Hnuc62Q130_provenance.
- NP762351.RAm-E22mgRJsiTfoy_iVmSVF5f-Tw3W96jpkz2Hnuc62Q130_assertion wasDerivedFrom befree-20150227 NP762351.RAm-E22mgRJsiTfoy_iVmSVF5f-Tw3W96jpkz2Hnuc62Q130_provenance.
- NP762351.RAm-E22mgRJsiTfoy_iVmSVF5f-Tw3W96jpkz2Hnuc62Q130_assertion SIO_000772 8988167 NP762351.RAm-E22mgRJsiTfoy_iVmSVF5f-Tw3W96jpkz2Hnuc62Q130_provenance.
- NP762351.RAm-E22mgRJsiTfoy_iVmSVF5f-Tw3W96jpkz2Hnuc62Q130_assertion evidence source_evidence_literature NP762351.RAm-E22mgRJsiTfoy_iVmSVF5f-Tw3W96jpkz2Hnuc62Q130_provenance.
- NP762351.RAm-E22mgRJsiTfoy_iVmSVF5f-Tw3W96jpkz2Hnuc62Q130_assertion description "[Saethre-Chotzen syndrome (acrocephalo-syndactyly type III, ACS III) is an autosomal dominant craniosynostosis with brachydactyly, soft tissue syndactyly and facial dysmorphism including ptosis, facial asymmetry and prominent ear crura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762351.RAm-E22mgRJsiTfoy_iVmSVF5f-Tw3W96jpkz2Hnuc62Q130_provenance.