Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_provenance.
- NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_assertion description "[The mutation screening of PTPN22 in AD patients (n=332) and controls (n=112) revealed eight missense variants, five of which have not been reported previously.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_provenance.
- NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_assertion evidence source_evidence_literature NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_provenance.
- NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_assertion SIO_000772 18301444 NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_provenance.
- NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_assertion wasDerivedFrom befree-20140225 NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_provenance.
- NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_assertion wasGeneratedBy ECO_0000203 NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP432740.RAEztUvGe9WfkceO5mT7q2QrwjF1CCWRbVaEA6cbBtlR4130_provenance.