Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_provenance.
- befree-2016 importedOn "2016-02-19" NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_provenance.
- NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_assertion wasGeneratedBy ECO_0000203 NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_provenance.
- NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_assertion wasDerivedFrom befree-2016 NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_provenance.
- NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_assertion SIO_000772 16638984 NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_provenance.
- NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_assertion evidence source_evidence_literature NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_provenance.
- NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_assertion description "[Recently, the CYP1B1 gene was found to be associated with Peters' anomaly, and the gene associated with oculodentodigital dysplasia syndrome, which presents some similarities with AR, was identified (connexin 43--GJA1 gene).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP546787.RAT-pUKUbsRWBhmmISLkMFKqz_L_A-qRf-czK_N7tojFI130_provenance.