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- source_evidence_literature type ECO_0000212 NP172955.RAmwwu0RUySKqYxF_fqkOL3z95mcRhy91p7imDyvTJ9oY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP172955.RAmwwu0RUySKqYxF_fqkOL3z95mcRhy91p7imDyvTJ9oY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP172955.RAmwwu0RUySKqYxF_fqkOL3z95mcRhy91p7imDyvTJ9oY130_provenance.
- NP172955.RAmwwu0RUySKqYxF_fqkOL3z95mcRhy91p7imDyvTJ9oY130_assertion description "[The findings suggest that polymorphisms of MDM2 and TP53 genes may be genetic modifier for developing NPC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172955.RAmwwu0RUySKqYxF_fqkOL3z95mcRhy91p7imDyvTJ9oY130_provenance.
- NP172955.RAmwwu0RUySKqYxF_fqkOL3z95mcRhy91p7imDyvTJ9oY130_assertion evidence source_evidence_literature NP172955.RAmwwu0RUySKqYxF_fqkOL3z95mcRhy91p7imDyvTJ9oY130_provenance.
- NP172955.RAmwwu0RUySKqYxF_fqkOL3z95mcRhy91p7imDyvTJ9oY130_assertion SIO_000772 20398418 NP172955.RAmwwu0RUySKqYxF_fqkOL3z95mcRhy91p7imDyvTJ9oY130_provenance.
- NP172955.RAmwwu0RUySKqYxF_fqkOL3z95mcRhy91p7imDyvTJ9oY130_assertion wasDerivedFrom gad-20150221 NP172955.RAmwwu0RUySKqYxF_fqkOL3z95mcRhy91p7imDyvTJ9oY130_provenance.
- NP172955.RAmwwu0RUySKqYxF_fqkOL3z95mcRhy91p7imDyvTJ9oY130_assertion wasGeneratedBy ECO_0000203 NP172955.RAmwwu0RUySKqYxF_fqkOL3z95mcRhy91p7imDyvTJ9oY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP172955.RAmwwu0RUySKqYxF_fqkOL3z95mcRhy91p7imDyvTJ9oY130_provenance.