Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_provenance.
- NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_assertion description "[Our results show, for the first time that MSC from MDS display genomic aberrations, assessed by array-CGH and FISH, some of them specially linked to a particular MDS subtype, the 5q- syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_provenance.
- NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_assertion evidence source_evidence_literature NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_provenance.
- NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_assertion SIO_000772 19151777 NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_provenance.
- NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_assertion wasDerivedFrom befree-2016 NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_provenance.
- NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_assertion wasGeneratedBy ECO_0000203 NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_provenance.
- befree-2016 importedOn "2016-02-19" NP715147.RAcQkVYSZw6wRb7p5aOc_yaeLFJHclilhBs9Rs4jMLC-U130_provenance.