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- source_evidence_literature type ECO_0000212 NP180156.RArY-pbAGjNgeIinjRAw9k4ulyyKSM2qlyeTi48RJJntM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP180156.RArY-pbAGjNgeIinjRAw9k4ulyyKSM2qlyeTi48RJJntM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP180156.RArY-pbAGjNgeIinjRAw9k4ulyyKSM2qlyeTi48RJJntM130_provenance.
- NP180156.RArY-pbAGjNgeIinjRAw9k4ulyyKSM2qlyeTi48RJJntM130_assertion description "[Bi-allelic germline mutations of the Fanconi anemia (FA) genes, PALB2/FANCN and BRCA2/FANCD1, have been reported in a few Wilms tumor (WT) patients with an atypical FA phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180156.RArY-pbAGjNgeIinjRAw9k4ulyyKSM2qlyeTi48RJJntM130_provenance.
- NP180156.RArY-pbAGjNgeIinjRAw9k4ulyyKSM2qlyeTi48RJJntM130_assertion evidence source_evidence_literature NP180156.RArY-pbAGjNgeIinjRAw9k4ulyyKSM2qlyeTi48RJJntM130_provenance.
- NP180156.RArY-pbAGjNgeIinjRAw9k4ulyyKSM2qlyeTi48RJJntM130_assertion SIO_000772 20589654 NP180156.RArY-pbAGjNgeIinjRAw9k4ulyyKSM2qlyeTi48RJJntM130_provenance.
- NP180156.RArY-pbAGjNgeIinjRAw9k4ulyyKSM2qlyeTi48RJJntM130_assertion wasDerivedFrom gad-20150221 NP180156.RArY-pbAGjNgeIinjRAw9k4ulyyKSM2qlyeTi48RJJntM130_provenance.
- NP180156.RArY-pbAGjNgeIinjRAw9k4ulyyKSM2qlyeTi48RJJntM130_assertion wasGeneratedBy ECO_0000203 NP180156.RArY-pbAGjNgeIinjRAw9k4ulyyKSM2qlyeTi48RJJntM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP180156.RArY-pbAGjNgeIinjRAw9k4ulyyKSM2qlyeTi48RJJntM130_provenance.