Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_provenance.
- NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_assertion description "[Frequencies of methylation in GCTs were 7/25 (28 % for FHIT), 6/25 (24% for FNACF), 3/25 (12% for Cyclin D2), 1/25 (4% for BRCA2) and 14/25 (56%) in RUNX3 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_provenance.
- NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_assertion evidence source_evidence_literature NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_provenance.
- NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_assertion SIO_000772 15574200 NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_provenance.
- NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_assertion wasDerivedFrom befree-20140225 NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_provenance.
- NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_assertion wasGeneratedBy ECO_0000203 NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP775333.RAzCU3d29fsUM6Jb0lCj9jp8CTMj56Lc1A-lTcas4KjGA130_provenance.