Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_provenance.
- NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_assertion description "[The cell line established from nodule (SCID 5019 p11), showed a number of new changes, as described; however, the most significant change was amplification of the 8q23 approximately qter region, harboring c-myc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_provenance.
- NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_assertion evidence source_evidence_literature NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_provenance.
- NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_assertion SIO_000772 10942801 NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_provenance.
- NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_assertion wasDerivedFrom befree-20140225 NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_provenance.
- NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_assertion wasGeneratedBy ECO_0000203 NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP240051.RAcVcsLb5PwvYEdvG9CCNXRVaQpKmzFompisSHFlw0Jqg130_provenance.