Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_provenance.
- NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_assertion description "[Besides E-cadherin loss, the best known ILC genetic hallmark, we identified mutations targeting PTEN, TBX3, and FOXA1 as ILC enriched features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_provenance.
- NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_assertion evidence source_evidence_literature NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_provenance.
- NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_assertion SIO_000772 26451490 NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_provenance.
- NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_assertion wasDerivedFrom befree-2016 NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_provenance.
- NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_assertion wasGeneratedBy ECO_0000203 NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1294812.RApmBUxuw0Nl_oEqtTaG4Q2t9oXPRuMuDZgbtCbdixwtg130_provenance.