Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_provenance.
- NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_assertion wasGeneratedBy ECO_0000203 NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_provenance.
- NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_assertion wasDerivedFrom befree-20150227 NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_provenance.
- NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_assertion SIO_000772 16638984 NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_provenance.
- NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_assertion evidence source_evidence_literature NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_provenance.
- NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_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." NP425587.RALvR9dhm_rH0bolQsNP2p-IRX52oufMSN6Gf6b8wTnGk130_provenance.