Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_provenance.
- NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_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." NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_provenance.
- NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_assertion evidence source_evidence_literature NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_provenance.
- NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_assertion SIO_000772 19151777 NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_provenance.
- NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_assertion wasDerivedFrom befree-20140225 NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_provenance.
- NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_assertion wasGeneratedBy ECO_0000203 NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP707691.RA4vVoptt9wsJH0-B6bKJroDd24-KpdG15m9lLvyOwWuU130_provenance.