Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_provenance.
- NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_assertion description "[Positional candidate gene approaches have identified TSGs within two of these regions, i.e., p16/CDKN2A at 9p21 and NF2 at 22q12, which are frequently altered in MMs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_provenance.
- NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_assertion evidence source_evidence_literature NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_provenance.
- NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_assertion SIO_000772 9863027 NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_provenance.
- NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_assertion wasDerivedFrom befree-20140225 NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_provenance.
- NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_assertion wasGeneratedBy ECO_0000203 NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP722996.RArOy_WyaIfJLzPZbJAXSJRxsDkxWjkN9RZlTESNc1CSI130_provenance.