Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_provenance.
- NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_assertion description "[A 27 base-pair deletion of the anti-m�llerian type II receptor gene is the most common cause of the persistent m�llerian duct syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_provenance.
- NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_assertion evidence source_evidence_curated NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_provenance.
- NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_assertion SIO_000772 8872466 NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_provenance.
- NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_assertion wasDerivedFrom uniprot-2016 NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_provenance.
- NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_assertion wasGeneratedBy ECO_0000218 NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9189.RATb5gm8_ujUOKr9YIlmfnqSNFJoI4qGPbvgg7rLKXZTg130_provenance.