Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_assertion> ?p ?o ?g. }
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- NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_assertion type Assertion NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_head.
- NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_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." NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_provenance.
- NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_assertion evidence source_evidence_literature NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_provenance.
- NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_assertion SIO_000772 15916101 NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_provenance.
- NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_assertion wasDerivedFrom befree-20140225 NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_provenance.
- NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_assertion wasGeneratedBy ECO_0000203 NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_provenance.