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- source_evidence_literature type ECO_0000212 NP601299.RAWG-98U6BHOR4bCC_AV_BLHVn9mdGZ7ih3nNvv8aVabA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP601299.RAWG-98U6BHOR4bCC_AV_BLHVn9mdGZ7ih3nNvv8aVabA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP601299.RAWG-98U6BHOR4bCC_AV_BLHVn9mdGZ7ih3nNvv8aVabA130_provenance.
- NP601299.RAWG-98U6BHOR4bCC_AV_BLHVn9mdGZ7ih3nNvv8aVabA130_assertion description "[(Nature 352, 539-540) demonstrated that the GLI3 gene in 7p13 was disrupted in, patients with Greig syndrome and, more recently, the linkage of genetic markers from 7p with the Saethre-Chotzen syndrome locus has been reported (2,3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601299.RAWG-98U6BHOR4bCC_AV_BLHVn9mdGZ7ih3nNvv8aVabA130_provenance.
- NP601299.RAWG-98U6BHOR4bCC_AV_BLHVn9mdGZ7ih3nNvv8aVabA130_assertion evidence source_evidence_literature NP601299.RAWG-98U6BHOR4bCC_AV_BLHVn9mdGZ7ih3nNvv8aVabA130_provenance.
- NP601299.RAWG-98U6BHOR4bCC_AV_BLHVn9mdGZ7ih3nNvv8aVabA130_assertion SIO_000772 7987323 NP601299.RAWG-98U6BHOR4bCC_AV_BLHVn9mdGZ7ih3nNvv8aVabA130_provenance.
- NP601299.RAWG-98U6BHOR4bCC_AV_BLHVn9mdGZ7ih3nNvv8aVabA130_assertion wasDerivedFrom befree-20140225 NP601299.RAWG-98U6BHOR4bCC_AV_BLHVn9mdGZ7ih3nNvv8aVabA130_provenance.
- NP601299.RAWG-98U6BHOR4bCC_AV_BLHVn9mdGZ7ih3nNvv8aVabA130_assertion wasGeneratedBy ECO_0000203 NP601299.RAWG-98U6BHOR4bCC_AV_BLHVn9mdGZ7ih3nNvv8aVabA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP601299.RAWG-98U6BHOR4bCC_AV_BLHVn9mdGZ7ih3nNvv8aVabA130_provenance.