Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP336367.RAOfx7ZEFYb4hNXqPEnTeZUCw9hxnADuh51yp0q8Y5voE130_assertion> ?p ?o ?g. }
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- NP336367.RAOfx7ZEFYb4hNXqPEnTeZUCw9hxnADuh51yp0q8Y5voE130_assertion type Assertion NP336367.RAOfx7ZEFYb4hNXqPEnTeZUCw9hxnADuh51yp0q8Y5voE130_head.
- NP336367.RAOfx7ZEFYb4hNXqPEnTeZUCw9hxnADuh51yp0q8Y5voE130_assertion description "[BBS2 is a clinically and genetically heterogeneous group of disorders resulting in rod-cone dystrophy, obesity, postaxial polydactyly, renal dysfunction, and mental retardation, which were very recently associated with a novel gene designated BBS2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP336367.RAOfx7ZEFYb4hNXqPEnTeZUCw9hxnADuh51yp0q8Y5voE130_provenance.
- NP336367.RAOfx7ZEFYb4hNXqPEnTeZUCw9hxnADuh51yp0q8Y5voE130_assertion evidence source_evidence_literature NP336367.RAOfx7ZEFYb4hNXqPEnTeZUCw9hxnADuh51yp0q8Y5voE130_provenance.
- NP336367.RAOfx7ZEFYb4hNXqPEnTeZUCw9hxnADuh51yp0q8Y5voE130_assertion SIO_000772 11707781 NP336367.RAOfx7ZEFYb4hNXqPEnTeZUCw9hxnADuh51yp0q8Y5voE130_provenance.
- NP336367.RAOfx7ZEFYb4hNXqPEnTeZUCw9hxnADuh51yp0q8Y5voE130_assertion wasDerivedFrom befree-2016 NP336367.RAOfx7ZEFYb4hNXqPEnTeZUCw9hxnADuh51yp0q8Y5voE130_provenance.
- NP336367.RAOfx7ZEFYb4hNXqPEnTeZUCw9hxnADuh51yp0q8Y5voE130_assertion wasGeneratedBy ECO_0000203 NP336367.RAOfx7ZEFYb4hNXqPEnTeZUCw9hxnADuh51yp0q8Y5voE130_provenance.