Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_provenance.
- NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_assertion description "[We demonstrate that necdin and Magel2 bind to and prevent proteasomal degradation of Fez1, a fasciculation and elongation protein implicated in axonal outgrowth and kinesin-mediated transport, and also bind to the Bardet-Biedl syndrome (BBS) protein BBS4 in co-transfected cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_provenance.
- NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_assertion evidence source_evidence_literature NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_provenance.
- NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_assertion SIO_000772 15649943 NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_provenance.
- NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_assertion wasDerivedFrom befree-20150227 NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_provenance.
- NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_assertion wasGeneratedBy ECO_0000203 NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP912047.RAv1b80isvIBtGKEjx95KqmXRIBT0lp026Dxb6hGna5Rw130_provenance.