Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_provenance.
- NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_assertion description "[This family demonstrates some of the phenotypic features of the multiple endocrine neoplasia type 2B syndrome without the characteristic neoplasms or the mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_provenance.
- NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_assertion evidence source_evidence_literature NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_provenance.
- NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_assertion SIO_000772 7573303 NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_provenance.
- NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_assertion wasDerivedFrom befree-2016 NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_provenance.
- NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_assertion wasGeneratedBy ECO_0000203 NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_provenance.
- befree-2016 importedOn "2016-02-19" NP1313040.RA75rnw0FLFvbe6iIW-pCf3nAWjD-WRFL_jcLEyC3DX2E130_provenance.