Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_provenance.
- NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_assertion wasGeneratedBy ECO_0000203 NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_provenance.
- NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_assertion wasDerivedFrom befree-20150227 NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_provenance.
- NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_assertion SIO_000772 21683322 NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_provenance.
- NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_assertion evidence source_evidence_literature NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_provenance.
- NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_assertion description "[After exome sequencing in GD and AD cases, we selected fibrillin 1 (FBN1) as a candidate gene, even though mutations in this gene have been described in Marfan syndrome, which is characterized by tall stature and arachnodactyly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395725.RANa2EJrSmaTL4Ws1cJcx-6XsIEIC3xVIZpzcSxkeNnHI130_provenance.