Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP789494.RAO90jPBskzCpb5PhQZRWiQbnuhb2ZH0UCDZUvChVFKZ4130_assertion> ?p ?o ?g. }
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- NP789494.RAO90jPBskzCpb5PhQZRWiQbnuhb2ZH0UCDZUvChVFKZ4130_assertion type Assertion NP789494.RAO90jPBskzCpb5PhQZRWiQbnuhb2ZH0UCDZUvChVFKZ4130_head.
- NP789494.RAO90jPBskzCpb5PhQZRWiQbnuhb2ZH0UCDZUvChVFKZ4130_assertion wasGeneratedBy ECO_0000203 NP789494.RAO90jPBskzCpb5PhQZRWiQbnuhb2ZH0UCDZUvChVFKZ4130_provenance.
- NP789494.RAO90jPBskzCpb5PhQZRWiQbnuhb2ZH0UCDZUvChVFKZ4130_assertion wasDerivedFrom befree-2016 NP789494.RAO90jPBskzCpb5PhQZRWiQbnuhb2ZH0UCDZUvChVFKZ4130_provenance.
- NP789494.RAO90jPBskzCpb5PhQZRWiQbnuhb2ZH0UCDZUvChVFKZ4130_assertion SIO_000772 20101889 NP789494.RAO90jPBskzCpb5PhQZRWiQbnuhb2ZH0UCDZUvChVFKZ4130_provenance.
- NP789494.RAO90jPBskzCpb5PhQZRWiQbnuhb2ZH0UCDZUvChVFKZ4130_assertion evidence source_evidence_literature NP789494.RAO90jPBskzCpb5PhQZRWiQbnuhb2ZH0UCDZUvChVFKZ4130_provenance.
- NP789494.RAO90jPBskzCpb5PhQZRWiQbnuhb2ZH0UCDZUvChVFKZ4130_assertion description "[Thyroid peroxidase gene mutations causing congenital hypothyroidism in three Turkish families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789494.RAO90jPBskzCpb5PhQZRWiQbnuhb2ZH0UCDZUvChVFKZ4130_provenance.