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- source_evidence_literature type ECO_0000212 NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_provenance.
- NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_assertion wasGeneratedBy ECO_0000203 NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_provenance.
- NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_assertion wasDerivedFrom befree-2016 NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_provenance.
- NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_assertion SIO_000772 9393760 NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_provenance.
- NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_assertion evidence source_evidence_literature NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_provenance.
- NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_assertion description "[We have determined the genomic organization and intron/exon boundaries of Hel-N1 and have screened the entire coding region for mutations by sequencing 14 primary SCLCs and cell lines and 21 primary NSCLCs preselected for localized 9p21 deletion or monosomy of chromosome 9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_provenance.