Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_provenance.
- NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_assertion description "[We reported recently an increase in the frequency of loss of 7q33-q35 between LGD and HGD as determined by comparative genomic hybridization (P. H. J. Riegman et al., Cancer Res., 61: 3164-3170, 2001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_provenance.
- NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_assertion evidence source_evidence_literature NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_provenance.
- NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_assertion SIO_000772 11888931 NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_provenance.
- NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_assertion wasDerivedFrom befree-20140225 NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_provenance.
- NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_assertion wasGeneratedBy ECO_0000203 NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP242508.RACdwBVXLPyriF7DqyyN95cUde9FSYHv5ZWcEz0cVHeVQ130_provenance.