Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_provenance.
- NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_assertion description "[Focusing on cytogenetic aberrations most commonly found in MDS, we retrospectively genotyped 566 MDS/AML patients carrying -5/del(5q), -7/del(7q), +8, del(20q) and -Y.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_provenance.
- NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_assertion evidence source_evidence_literature NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_provenance.
- NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_assertion SIO_000772 23643325 NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_provenance.
- NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_assertion wasDerivedFrom befree-2016 NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_provenance.
- NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_assertion wasGeneratedBy ECO_0000203 NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1074852.RAUa9QLxNK8sLvv6zUD5JPuzDsVzgppDE1dB7rCE-DxLI130_provenance.