Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_provenance.
- NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_assertion description "[Mutational screening of the RET gene identified a common mutation (C618R) in all 8 (7 FMTC and 1 MEN2A) unrelated Cypriot patients which may be explained by a founder effect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_provenance.
- NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_assertion evidence source_evidence_literature NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_provenance.
- NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_assertion SIO_000772 21422799 NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_provenance.
- NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_assertion wasDerivedFrom befree-2016 NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_provenance.
- NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_assertion wasGeneratedBy ECO_0000203 NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_provenance.
- befree-2016 importedOn "2016-02-19" NP881056.RA8hWzzWBptlTSgo36_4BimMnYfIY3wxUJpH9JadTx5yY130_provenance.