Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_provenance.
- NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_assertion wasGeneratedBy ECO_0000203 NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_provenance.
- NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_assertion wasDerivedFrom befree-2016 NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_provenance.
- NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_assertion SIO_000772 9783714 NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_provenance.
- NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_assertion evidence source_evidence_literature NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_provenance.
- NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_assertion description "[While mosaicism alone might have accounted for the phenotypic differences, by PCR analysis the Turner syndrome patient was SRY and ZFY negative and the mixed gonadal dysgenesis patient was SRY and ZFY positive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1406373.RAtZHDM12t7FtbrEqgWrEMY2gt9SibGJgwxXGh0VI78sk130_provenance.