Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_provenance.
- NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_assertion wasGeneratedBy ECO_0000203 NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_provenance.
- NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_assertion wasDerivedFrom befree-20140225 NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_provenance.
- NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_assertion SIO_000772 11935336 NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_provenance.
- NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_assertion evidence source_evidence_literature NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_provenance.
- NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_assertion description "[We describe the analysis of the chromosome breakpoints in a patient with congenital bilateral isolated ptosis and a de novo balanced translocation 46,XY,t(1;8)(p34.3;q21.12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP223668.RAd3c-oGLpFvjIBwEIdjRWtaayPwYWm2GiKlY4AMa6aPY130_provenance.