Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance.
- NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_assertion wasGeneratedBy ECO_0000203 NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance.
- NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_assertion wasDerivedFrom befree-20140225 NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance.
- NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_assertion SIO_000772 19473076 NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance.
- NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_assertion evidence source_evidence_literature NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance.
- NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_assertion description "[Congenital contractural arachnodactyly (Beals syndrome) is a rare autosomal dominantly inherited connective tissue disorder characterized by flexion contractures, arachnodactyly, crumpled ears, and mild muscular hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance.
- befree-20140225 importedOn "2014-02-25" NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance.