Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_provenance.
- befree-2016 importedOn "2016-02-19" NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_provenance.
- NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_assertion wasGeneratedBy ECO_0000203 NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_provenance.
- NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_assertion wasDerivedFrom befree-2016 NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_provenance.
- NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_assertion SIO_000772 22512561 NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_provenance.
- NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_assertion evidence source_evidence_literature NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_provenance.
- NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_provenance.