Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP741279.RAkmsrNxIgeZPyWrPvOdlKM6Yy19Cymzz8JmpnJccvWjg130_assertion> ?p ?o ?g. }
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- NP741279.RAkmsrNxIgeZPyWrPvOdlKM6Yy19Cymzz8JmpnJccvWjg130_assertion type Assertion NP741279.RAkmsrNxIgeZPyWrPvOdlKM6Yy19Cymzz8JmpnJccvWjg130_head.
- NP741279.RAkmsrNxIgeZPyWrPvOdlKM6Yy19Cymzz8JmpnJccvWjg130_assertion wasGeneratedBy ECO_0000203 NP741279.RAkmsrNxIgeZPyWrPvOdlKM6Yy19Cymzz8JmpnJccvWjg130_provenance.
- NP741279.RAkmsrNxIgeZPyWrPvOdlKM6Yy19Cymzz8JmpnJccvWjg130_assertion wasDerivedFrom befree-2016 NP741279.RAkmsrNxIgeZPyWrPvOdlKM6Yy19Cymzz8JmpnJccvWjg130_provenance.
- NP741279.RAkmsrNxIgeZPyWrPvOdlKM6Yy19Cymzz8JmpnJccvWjg130_assertion SIO_000772 19473076 NP741279.RAkmsrNxIgeZPyWrPvOdlKM6Yy19Cymzz8JmpnJccvWjg130_provenance.
- NP741279.RAkmsrNxIgeZPyWrPvOdlKM6Yy19Cymzz8JmpnJccvWjg130_assertion evidence source_evidence_literature NP741279.RAkmsrNxIgeZPyWrPvOdlKM6Yy19Cymzz8JmpnJccvWjg130_provenance.
- NP741279.RAkmsrNxIgeZPyWrPvOdlKM6Yy19Cymzz8JmpnJccvWjg130_assertion description "[Congenital contractural arachnodactyly (Beals syndrome) is a rare autosomal dominantly inherited connective tissue disorder characterized by flexion contractures, arachnodactyly, crumpled ears, and mild muscular hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP741279.RAkmsrNxIgeZPyWrPvOdlKM6Yy19Cymzz8JmpnJccvWjg130_provenance.