Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP61146.RA8C2g7ezYLt3wTJqvgz2i2lsoGdAcoZ5uw3sYb61Jyds130_assertion> ?p ?o ?g. }
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- NP61146.RA8C2g7ezYLt3wTJqvgz2i2lsoGdAcoZ5uw3sYb61Jyds130_assertion type Assertion NP61146.RA8C2g7ezYLt3wTJqvgz2i2lsoGdAcoZ5uw3sYb61Jyds130_head.
- NP61146.RA8C2g7ezYLt3wTJqvgz2i2lsoGdAcoZ5uw3sYb61Jyds130_assertion description "[Our study demonstrates that mutations in each part of the EGFR pathway were associated with different clinicopathologic features in patients with NSCLCs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP61146.RA8C2g7ezYLt3wTJqvgz2i2lsoGdAcoZ5uw3sYb61Jyds130_provenance.
- NP61146.RA8C2g7ezYLt3wTJqvgz2i2lsoGdAcoZ5uw3sYb61Jyds130_assertion evidence source_evidence_literature NP61146.RA8C2g7ezYLt3wTJqvgz2i2lsoGdAcoZ5uw3sYb61Jyds130_provenance.
- NP61146.RA8C2g7ezYLt3wTJqvgz2i2lsoGdAcoZ5uw3sYb61Jyds130_assertion SIO_000772 20881644 NP61146.RA8C2g7ezYLt3wTJqvgz2i2lsoGdAcoZ5uw3sYb61Jyds130_provenance.
- NP61146.RA8C2g7ezYLt3wTJqvgz2i2lsoGdAcoZ5uw3sYb61Jyds130_assertion wasDerivedFrom gad-20130706 NP61146.RA8C2g7ezYLt3wTJqvgz2i2lsoGdAcoZ5uw3sYb61Jyds130_provenance.
- NP61146.RA8C2g7ezYLt3wTJqvgz2i2lsoGdAcoZ5uw3sYb61Jyds130_assertion wasGeneratedBy ECO_0000203 NP61146.RA8C2g7ezYLt3wTJqvgz2i2lsoGdAcoZ5uw3sYb61Jyds130_provenance.