Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_provenance.
- NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_assertion description "[We report two unrelated patients with MWS where the clinical diagnosis was established only after finding of disruption of the ZEB2 gene by a balanced translocation breakpoint and an interstitial microdeletion, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_provenance.
- NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_assertion evidence source_evidence_literature NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_provenance.
- NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_assertion SIO_000772 18445050 NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_provenance.
- NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_assertion wasDerivedFrom befree-2016 NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_provenance.
- NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_assertion wasGeneratedBy ECO_0000203 NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_provenance.
- befree-2016 importedOn "2016-02-19" NP668464.RAXr7q2atvn1iaRHWuflAzYxeUglVhImt4D7tkYtYsZys130_provenance.