Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_provenance.
- NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_assertion description "[EGFR-mutated adenocarcinomas displayed a larger number of copy number alterations and recurrent amplifications, a higher fraction of total loss-of-heterozygosity, higher genomic complexity, and a more distinct expression pattern than EGFR-wild type adenocarcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_provenance.
- NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_assertion evidence source_evidence_literature NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_provenance.
- NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_assertion SIO_000772 24205279 NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_provenance.
- NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_assertion wasDerivedFrom befree-2016 NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_provenance.
- NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_assertion wasGeneratedBy ECO_0000203 NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_provenance.
- befree-2016 importedOn "2016-02-19" NP1126312.RABypTTachdGbn1lKu10lg5g1PfgGVjoj0hmaUh-WJ2ko130_provenance.