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- source_evidence_literature type ECO_0000212 NP940479.RAdWn4sNRHsh-AnUPC0EqBNwf2m9ZOgVrI1dKkpCqJVsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP940479.RAdWn4sNRHsh-AnUPC0EqBNwf2m9ZOgVrI1dKkpCqJVsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP940479.RAdWn4sNRHsh-AnUPC0EqBNwf2m9ZOgVrI1dKkpCqJVsU130_provenance.
- NP940479.RAdWn4sNRHsh-AnUPC0EqBNwf2m9ZOgVrI1dKkpCqJVsU130_assertion description "[The EGFR mutation is rare in SCLC patients, and EGFR mutation might occur more often in combined SCLCs than conventional patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP940479.RAdWn4sNRHsh-AnUPC0EqBNwf2m9ZOgVrI1dKkpCqJVsU130_provenance.
- NP940479.RAdWn4sNRHsh-AnUPC0EqBNwf2m9ZOgVrI1dKkpCqJVsU130_assertion evidence source_evidence_literature NP940479.RAdWn4sNRHsh-AnUPC0EqBNwf2m9ZOgVrI1dKkpCqJVsU130_provenance.
- NP940479.RAdWn4sNRHsh-AnUPC0EqBNwf2m9ZOgVrI1dKkpCqJVsU130_assertion SIO_000772 22103903 NP940479.RAdWn4sNRHsh-AnUPC0EqBNwf2m9ZOgVrI1dKkpCqJVsU130_provenance.
- NP940479.RAdWn4sNRHsh-AnUPC0EqBNwf2m9ZOgVrI1dKkpCqJVsU130_assertion wasDerivedFrom befree-2016 NP940479.RAdWn4sNRHsh-AnUPC0EqBNwf2m9ZOgVrI1dKkpCqJVsU130_provenance.
- NP940479.RAdWn4sNRHsh-AnUPC0EqBNwf2m9ZOgVrI1dKkpCqJVsU130_assertion wasGeneratedBy ECO_0000203 NP940479.RAdWn4sNRHsh-AnUPC0EqBNwf2m9ZOgVrI1dKkpCqJVsU130_provenance.
- befree-2016 importedOn "2016-02-19" NP940479.RAdWn4sNRHsh-AnUPC0EqBNwf2m9ZOgVrI1dKkpCqJVsU130_provenance.