Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_assertion> ?p ?o ?g. }
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- NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_assertion type Assertion NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_head.
- NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_provenance.
- NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_assertion evidence source_evidence_literature NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_provenance.
- NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_assertion SIO_000772 16000300 NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_provenance.
- NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_assertion wasDerivedFrom befree-2016 NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_provenance.
- NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_assertion wasGeneratedBy ECO_0000203 NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_provenance.