Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_provenance.
- NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_assertion description "[The presence of variant alleles in NER genes increases risk of esophageal adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_provenance.
- NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_assertion evidence source_evidence_literature NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_provenance.
- NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_assertion SIO_000772 18478337 NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_provenance.
- NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_assertion wasDerivedFrom gad-20150221 NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_provenance.
- NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_assertion wasGeneratedBy ECO_0000203 NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP123049.RAaUNoeD_aRmYNoKVNmuk_5Ld08JbhGiX6AXoTw2fnlbg130_provenance.