Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_provenance.
- NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_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." NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_provenance.
- NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_assertion evidence source_evidence_literature NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_provenance.
- NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_assertion SIO_000772 15916101 NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_provenance.
- NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_assertion wasDerivedFrom befree-20140225 NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_provenance.
- NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_assertion wasGeneratedBy ECO_0000203 NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP812436.RAYH623by97WnzJWmW6t4uoJoIht5PcF-qlxmbJhdO-6Y130_provenance.