Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_provenance.
- NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_assertion description "[Exon19 deletions and exon21 L858R mutations in EGFR were detected in 4 (12%) and 13 (38%) of 34 NSCLC cases, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_provenance.
- NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_assertion evidence source_evidence_literature NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_provenance.
- NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_assertion SIO_000772 18448998 NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_provenance.
- NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_assertion wasDerivedFrom befree-2016 NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_provenance.
- NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_assertion wasGeneratedBy ECO_0000203 NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_provenance.
- befree-2016 importedOn "2016-02-19" NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_provenance.