Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_provenance.
- NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_assertion wasGeneratedBy ECO_0000203 NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_provenance.
- NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_assertion wasDerivedFrom befree-20140225 NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_provenance.
- NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_assertion SIO_000772 12383326 NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_provenance.
- NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_assertion evidence source_evidence_literature NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_provenance.
- NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_assertion description "[The principal features of CCA are a marfanoid habitus, multiple congenital contractures, camptodactyly, arachnodactyly, kyphoscoliosis, muscular hypoplasia, and external ear malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP836881.RAUgQLQ6B4xj0-xJR6Y9ZR--P21kWEwuTiA9aXxhW4C0E130_provenance.