Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_provenance.
- NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_assertion description "[Entire CAPN3 gene deletion in a patient with limb-girdle muscular dystrophy type 2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_provenance.
- NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_assertion evidence source_evidence_literature NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_provenance.
- NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_assertion SIO_000772 24715573 NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_provenance.
- NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_assertion wasDerivedFrom befree-20150227 NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_provenance.
- NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_assertion wasGeneratedBy ECO_0000203 NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP280400.RACtlpUdDT79z8fZ9L2MbEa2OApGLXePVrUE591FgcGcI130_provenance.