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- source_evidence_literature type ECO_0000212 NP885220.RADtk6PA0vK74j9VFsfmIiN-HLyXVozQmIc3CqIZwyKpY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP885220.RADtk6PA0vK74j9VFsfmIiN-HLyXVozQmIc3CqIZwyKpY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP885220.RADtk6PA0vK74j9VFsfmIiN-HLyXVozQmIc3CqIZwyKpY130_provenance.
- NP885220.RADtk6PA0vK74j9VFsfmIiN-HLyXVozQmIc3CqIZwyKpY130_assertion description "[To determine the relative contribution of ZIC3 mutations to both heterotaxy and isolated CHD, we screened the coding region of ZIC3 in 194 unrelated patients, including 61 patients with classic heterotaxy, 93 patients with heart defects characteristic of heterotaxy, and 11 patients with situs inversus totalis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP885220.RADtk6PA0vK74j9VFsfmIiN-HLyXVozQmIc3CqIZwyKpY130_provenance.
- NP885220.RADtk6PA0vK74j9VFsfmIiN-HLyXVozQmIc3CqIZwyKpY130_assertion evidence source_evidence_literature NP885220.RADtk6PA0vK74j9VFsfmIiN-HLyXVozQmIc3CqIZwyKpY130_provenance.
- NP885220.RADtk6PA0vK74j9VFsfmIiN-HLyXVozQmIc3CqIZwyKpY130_assertion SIO_000772 14681828 NP885220.RADtk6PA0vK74j9VFsfmIiN-HLyXVozQmIc3CqIZwyKpY130_provenance.
- NP885220.RADtk6PA0vK74j9VFsfmIiN-HLyXVozQmIc3CqIZwyKpY130_assertion wasDerivedFrom befree-20140225 NP885220.RADtk6PA0vK74j9VFsfmIiN-HLyXVozQmIc3CqIZwyKpY130_provenance.
- NP885220.RADtk6PA0vK74j9VFsfmIiN-HLyXVozQmIc3CqIZwyKpY130_assertion wasGeneratedBy ECO_0000203 NP885220.RADtk6PA0vK74j9VFsfmIiN-HLyXVozQmIc3CqIZwyKpY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP885220.RADtk6PA0vK74j9VFsfmIiN-HLyXVozQmIc3CqIZwyKpY130_provenance.