Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_provenance.
- NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_assertion description "[We investigated two single-nucleotide polymorphisms (SNPs) in PDCD1 and five polymorphisms in CTLA4 in 102 patients with AAV and 188 healthy controls (HC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_provenance.
- NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_assertion evidence source_evidence_literature NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_provenance.
- NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_assertion SIO_000772 18448390 NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_provenance.
- NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_assertion wasDerivedFrom befree-2016 NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_provenance.
- NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_assertion wasGeneratedBy ECO_0000203 NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_provenance.
- befree-2016 importedOn "2016-02-19" NP668667.RAENeT4l5TVMcsTzhRKU4Y6sQJU1qfbtHyzizr38_5_Ww130_provenance.