Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_provenance.
- NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_assertion description "[The common aberration found in these two t-MDS cases was the fragility of chromosome 5 and monosomy of chromosome 18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_provenance.
- NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_assertion evidence source_evidence_literature NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_provenance.
- NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_assertion SIO_000772 12505257 NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_provenance.
- NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_assertion wasDerivedFrom befree-20150227 NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_provenance.
- NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_assertion wasGeneratedBy ECO_0000203 NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914015.RAqjU-KSMaHJ1Ws9xVjjJTku4qV6NQM808xa03eUX2NM8130_provenance.