Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1365312.RATLgLNOUSIwL4E4i0Y0gaaRBRiwrE0IboMBOWDSy_xjE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1365312.RATLgLNOUSIwL4E4i0Y0gaaRBRiwrE0IboMBOWDSy_xjE130_assertion type Assertion NP1365312.RATLgLNOUSIwL4E4i0Y0gaaRBRiwrE0IboMBOWDSy_xjE130_head.
- NP1365312.RATLgLNOUSIwL4E4i0Y0gaaRBRiwrE0IboMBOWDSy_xjE130_assertion wasGeneratedBy ECO_0000203 NP1365312.RATLgLNOUSIwL4E4i0Y0gaaRBRiwrE0IboMBOWDSy_xjE130_provenance.
- NP1365312.RATLgLNOUSIwL4E4i0Y0gaaRBRiwrE0IboMBOWDSy_xjE130_assertion wasDerivedFrom befree-2016 NP1365312.RATLgLNOUSIwL4E4i0Y0gaaRBRiwrE0IboMBOWDSy_xjE130_provenance.
- NP1365312.RATLgLNOUSIwL4E4i0Y0gaaRBRiwrE0IboMBOWDSy_xjE130_assertion SIO_000772 8988167 NP1365312.RATLgLNOUSIwL4E4i0Y0gaaRBRiwrE0IboMBOWDSy_xjE130_provenance.
- NP1365312.RATLgLNOUSIwL4E4i0Y0gaaRBRiwrE0IboMBOWDSy_xjE130_assertion evidence source_evidence_literature NP1365312.RATLgLNOUSIwL4E4i0Y0gaaRBRiwrE0IboMBOWDSy_xjE130_provenance.
- NP1365312.RATLgLNOUSIwL4E4i0Y0gaaRBRiwrE0IboMBOWDSy_xjE130_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." NP1365312.RATLgLNOUSIwL4E4i0Y0gaaRBRiwrE0IboMBOWDSy_xjE130_provenance.