Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_assertion type Assertion NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_head.
- NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_assertion description "[Crouzon Syndrome is an autosomal dominant syndromic craniosynostosis characterized by premature closure of cranial sutures, exophthalmos, and midface hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_provenance.
- NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_assertion evidence source_evidence_literature NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_provenance.
- NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_assertion SIO_000772 15916101 NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_provenance.
- NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_assertion wasDerivedFrom befree-20140225 NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_provenance.
- NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_assertion wasGeneratedBy ECO_0000203 NP398116.RAMMibN5iVG0NESt7krBBPHQPJlZT__p5sR6A0EQVxOeo130_provenance.