Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_provenance.
- NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_assertion description "[Cytogenetic analysis of the diagnostic bone marrow (BM) specimen revealed two unrelated abnormal clones--one had a dicentric (7;9)(p11;p11), resulting in the deletion of 7p and 9p, and the other had only trisomy 8.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_provenance.
- NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_assertion evidence source_evidence_literature NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_provenance.
- NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_assertion SIO_000772 20633764 NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_provenance.
- NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_assertion wasDerivedFrom befree-20140225 NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_provenance.
- NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_assertion wasGeneratedBy ECO_0000203 NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP756101.RAIDOSfgKWczqTAd5WAkmJAUgPTFeWukExHE32LNXyhTs130_provenance.