Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_assertion> ?p ?o ?g. }
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- NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_assertion type Assertion NP668714.RAEXDbLKFVx9CW4Wg9rBJbAhgRQ9S3HnYWvPfmOxg_ClU130_head.
- 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.