Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP303806.RAwnft_3U2yjGUWZHg0RTWA5XY-Eyjgf5sAdTVTiUtgJ4130_provenance.