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- source_evidence_literature type ECO_0000212 NP757825.RAuGlgavZu0bS-er-e8zQtj5Ig2Ex6jmShuJjWjw0uDQw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP757825.RAuGlgavZu0bS-er-e8zQtj5Ig2Ex6jmShuJjWjw0uDQw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP757825.RAuGlgavZu0bS-er-e8zQtj5Ig2Ex6jmShuJjWjw0uDQw130_provenance.
- NP757825.RAuGlgavZu0bS-er-e8zQtj5Ig2Ex6jmShuJjWjw0uDQw130_assertion description "[We screened 120 children with sporadic multiple congenital anomalies and either growth or mental retardation for uniparental disomy (UPD) or subtelomeric deletions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP757825.RAuGlgavZu0bS-er-e8zQtj5Ig2Ex6jmShuJjWjw0uDQw130_provenance.
- NP757825.RAuGlgavZu0bS-er-e8zQtj5Ig2Ex6jmShuJjWjw0uDQw130_assertion evidence source_evidence_literature NP757825.RAuGlgavZu0bS-er-e8zQtj5Ig2Ex6jmShuJjWjw0uDQw130_provenance.
- NP757825.RAuGlgavZu0bS-er-e8zQtj5Ig2Ex6jmShuJjWjw0uDQw130_assertion SIO_000772 11702212 NP757825.RAuGlgavZu0bS-er-e8zQtj5Ig2Ex6jmShuJjWjw0uDQw130_provenance.
- NP757825.RAuGlgavZu0bS-er-e8zQtj5Ig2Ex6jmShuJjWjw0uDQw130_assertion wasDerivedFrom befree-20140225 NP757825.RAuGlgavZu0bS-er-e8zQtj5Ig2Ex6jmShuJjWjw0uDQw130_provenance.
- NP757825.RAuGlgavZu0bS-er-e8zQtj5Ig2Ex6jmShuJjWjw0uDQw130_assertion wasGeneratedBy ECO_0000203 NP757825.RAuGlgavZu0bS-er-e8zQtj5Ig2Ex6jmShuJjWjw0uDQw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP757825.RAuGlgavZu0bS-er-e8zQtj5Ig2Ex6jmShuJjWjw0uDQw130_provenance.