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- source_evidence_literature type ECO_0000212 NP986907.RAbUDK_EI8jgd1TM8kV0Z7oUsE-K051bwrX9J0POjnr8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP986907.RAbUDK_EI8jgd1TM8kV0Z7oUsE-K051bwrX9J0POjnr8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP986907.RAbUDK_EI8jgd1TM8kV0Z7oUsE-K051bwrX9J0POjnr8U130_provenance.
- NP986907.RAbUDK_EI8jgd1TM8kV0Z7oUsE-K051bwrX9J0POjnr8U130_assertion description "[These findings illustrate the value of SNP arrays for the detection of novel recurrent genomic alterations that may contribute to CLL/SLL onset or progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986907.RAbUDK_EI8jgd1TM8kV0Z7oUsE-K051bwrX9J0POjnr8U130_provenance.
- NP986907.RAbUDK_EI8jgd1TM8kV0Z7oUsE-K051bwrX9J0POjnr8U130_assertion evidence source_evidence_literature NP986907.RAbUDK_EI8jgd1TM8kV0Z7oUsE-K051bwrX9J0POjnr8U130_provenance.
- NP986907.RAbUDK_EI8jgd1TM8kV0Z7oUsE-K051bwrX9J0POjnr8U130_assertion SIO_000772 24704113 NP986907.RAbUDK_EI8jgd1TM8kV0Z7oUsE-K051bwrX9J0POjnr8U130_provenance.
- NP986907.RAbUDK_EI8jgd1TM8kV0Z7oUsE-K051bwrX9J0POjnr8U130_assertion wasDerivedFrom befree-20150227 NP986907.RAbUDK_EI8jgd1TM8kV0Z7oUsE-K051bwrX9J0POjnr8U130_provenance.
- NP986907.RAbUDK_EI8jgd1TM8kV0Z7oUsE-K051bwrX9J0POjnr8U130_assertion wasGeneratedBy ECO_0000203 NP986907.RAbUDK_EI8jgd1TM8kV0Z7oUsE-K051bwrX9J0POjnr8U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP986907.RAbUDK_EI8jgd1TM8kV0Z7oUsE-K051bwrX9J0POjnr8U130_provenance.