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- source_evidence_literature type ECO_0000212 NP696306.RA4UQkb9o0J2RA_BC8jPaVso--kekMAfLLGYlEQLirnXE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP696306.RA4UQkb9o0J2RA_BC8jPaVso--kekMAfLLGYlEQLirnXE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP696306.RA4UQkb9o0J2RA_BC8jPaVso--kekMAfLLGYlEQLirnXE130_provenance.
- NP696306.RA4UQkb9o0J2RA_BC8jPaVso--kekMAfLLGYlEQLirnXE130_assertion description "[In contrast, chromosome aberrations were seen in 79% of early MDS samples and 90% of RAEB/AML samples, and were not as widely distributed over the genome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP696306.RA4UQkb9o0J2RA_BC8jPaVso--kekMAfLLGYlEQLirnXE130_provenance.
- NP696306.RA4UQkb9o0J2RA_BC8jPaVso--kekMAfLLGYlEQLirnXE130_assertion evidence source_evidence_literature NP696306.RA4UQkb9o0J2RA_BC8jPaVso--kekMAfLLGYlEQLirnXE130_provenance.
- NP696306.RA4UQkb9o0J2RA_BC8jPaVso--kekMAfLLGYlEQLirnXE130_assertion SIO_000772 18832655 NP696306.RA4UQkb9o0J2RA_BC8jPaVso--kekMAfLLGYlEQLirnXE130_provenance.
- NP696306.RA4UQkb9o0J2RA_BC8jPaVso--kekMAfLLGYlEQLirnXE130_assertion wasDerivedFrom befree-2016 NP696306.RA4UQkb9o0J2RA_BC8jPaVso--kekMAfLLGYlEQLirnXE130_provenance.
- NP696306.RA4UQkb9o0J2RA_BC8jPaVso--kekMAfLLGYlEQLirnXE130_assertion wasGeneratedBy ECO_0000203 NP696306.RA4UQkb9o0J2RA_BC8jPaVso--kekMAfLLGYlEQLirnXE130_provenance.
- befree-2016 importedOn "2016-02-19" NP696306.RA4UQkb9o0J2RA_BC8jPaVso--kekMAfLLGYlEQLirnXE130_provenance.