Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_provenance.
- NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_assertion description "[Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_provenance.
- NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_assertion evidence source_evidence_literature NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_provenance.
- NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_assertion SIO_000772 8456828 NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_provenance.
- NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_assertion wasDerivedFrom befree-20140225 NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_provenance.
- NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_assertion wasGeneratedBy ECO_0000203 NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP189888.RAC4Ym_l6fhvvCAm3GdUeXfYj5jiQ9il7UNq1mCA31nZE130_provenance.