Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_provenance.
- NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_assertion description "[The occurrence of this chromosomal abnormality reinforces the concept of tumour suppressor gene hypothesis in some cases with familial MDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_provenance.
- NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_assertion evidence source_evidence_literature NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_provenance.
- NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_assertion SIO_000772 8217806 NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_provenance.
- NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_assertion wasDerivedFrom befree-20140225 NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_provenance.
- NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_assertion wasGeneratedBy ECO_0000203 NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP808152.RA2vUIk_iUuUzUVY96SnsMOvfjI0KTUok2lNtohpHubfA130_provenance.