Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_provenance.
- NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_assertion description "[The frequency of KRAS mutations and the preponderance of three types of mutations in codons 12 and 13 in a large, unselected cohort of metastatic CRC confirm the previous data of small and selected CRC samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_provenance.
- NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_assertion evidence source_evidence_literature NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_provenance.
- NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_assertion SIO_000772 19679400 NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_provenance.
- NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_assertion wasDerivedFrom befree-2016 NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_provenance.
- NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_assertion wasGeneratedBy ECO_0000203 NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP757465.RAiSFtqFOsXblmZVh4ZF2dJ7jdZo7xs99Me8F_XLyspkQ130_provenance.