Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_provenance.
- NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_assertion description "[Neither the VDR C352T nor the MPO G463A genotype had manifested association with the dysplasia and carcinoma of the disease, whereas the MTHFR 677TT genotype may be a genetic risk factor for esophageal dysplasia and carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_provenance.
- NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_assertion evidence source_evidence_literature NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_provenance.
- NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_assertion SIO_000772 18662591 NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_provenance.
- NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_assertion wasDerivedFrom gad-20150221 NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_provenance.
- NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_assertion wasGeneratedBy ECO_0000203 NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP127365.RAq48nh_X-IbHMN24EIPsX-Me6RS9rl1MvRnBqbhfQDBo130_provenance.