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- source_evidence_literature type ECO_0000212 NP1098015.RAWJ5SbDi3_o6agpmvWN5hLJaukihsOALkMP15ZCo45f0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1098015.RAWJ5SbDi3_o6agpmvWN5hLJaukihsOALkMP15ZCo45f0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1098015.RAWJ5SbDi3_o6agpmvWN5hLJaukihsOALkMP15ZCo45f0130_provenance.
- NP1098015.RAWJ5SbDi3_o6agpmvWN5hLJaukihsOALkMP15ZCo45f0130_assertion description "[This study suggests that EGFR kinase domain mutations and EML4-ALK translocations are radiosensitive NSCLC genotypes, and proposes a novel model to identify radiosensitive subtypes of NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1098015.RAWJ5SbDi3_o6agpmvWN5hLJaukihsOALkMP15ZCo45f0130_provenance.
- NP1098015.RAWJ5SbDi3_o6agpmvWN5hLJaukihsOALkMP15ZCo45f0130_assertion evidence source_evidence_literature NP1098015.RAWJ5SbDi3_o6agpmvWN5hLJaukihsOALkMP15ZCo45f0130_provenance.
- NP1098015.RAWJ5SbDi3_o6agpmvWN5hLJaukihsOALkMP15ZCo45f0130_assertion SIO_000772 23897899 NP1098015.RAWJ5SbDi3_o6agpmvWN5hLJaukihsOALkMP15ZCo45f0130_provenance.
- NP1098015.RAWJ5SbDi3_o6agpmvWN5hLJaukihsOALkMP15ZCo45f0130_assertion wasDerivedFrom befree-2016 NP1098015.RAWJ5SbDi3_o6agpmvWN5hLJaukihsOALkMP15ZCo45f0130_provenance.
- NP1098015.RAWJ5SbDi3_o6agpmvWN5hLJaukihsOALkMP15ZCo45f0130_assertion wasGeneratedBy ECO_0000203 NP1098015.RAWJ5SbDi3_o6agpmvWN5hLJaukihsOALkMP15ZCo45f0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1098015.RAWJ5SbDi3_o6agpmvWN5hLJaukihsOALkMP15ZCo45f0130_provenance.