Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_provenance.
- NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_assertion description "[Common genetic variants in candidate genes and risk of familial lymphoid malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_provenance.
- NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_assertion evidence source_evidence_literature NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_provenance.
- NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_assertion SIO_000772 19573080 NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_provenance.
- NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_assertion wasDerivedFrom gad-20150221 NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_provenance.
- NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_assertion wasGeneratedBy ECO_0000203 NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP151577.RAo7p0aIto3mSz7VO_sxG5_OeKEOTNT0j7CL-MkQ_NNCo130_provenance.