Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP202121.RAvqLfNsJgtUnFQDFQn1ex8Bb-_QvSD832dP9C3X5LoQo130_assertion> ?p ?o ?g. }
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- NP202121.RAvqLfNsJgtUnFQDFQn1ex8Bb-_QvSD832dP9C3X5LoQo130_assertion type Assertion NP202121.RAvqLfNsJgtUnFQDFQn1ex8Bb-_QvSD832dP9C3X5LoQo130_head.
- NP202121.RAvqLfNsJgtUnFQDFQn1ex8Bb-_QvSD832dP9C3X5LoQo130_assertion description "[The 208delG mutation in the FSCN2 gene produces not only autosomal dominant retinitis pigmentosa but also ADMD (autosomal dominant macular degeneration) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP202121.RAvqLfNsJgtUnFQDFQn1ex8Bb-_QvSD832dP9C3X5LoQo130_provenance.
- NP202121.RAvqLfNsJgtUnFQDFQn1ex8Bb-_QvSD832dP9C3X5LoQo130_assertion evidence source_evidence_literature NP202121.RAvqLfNsJgtUnFQDFQn1ex8Bb-_QvSD832dP9C3X5LoQo130_provenance.
- NP202121.RAvqLfNsJgtUnFQDFQn1ex8Bb-_QvSD832dP9C3X5LoQo130_assertion SIO_000772 14609921 NP202121.RAvqLfNsJgtUnFQDFQn1ex8Bb-_QvSD832dP9C3X5LoQo130_provenance.
- NP202121.RAvqLfNsJgtUnFQDFQn1ex8Bb-_QvSD832dP9C3X5LoQo130_assertion wasDerivedFrom lhgdn-20090331 NP202121.RAvqLfNsJgtUnFQDFQn1ex8Bb-_QvSD832dP9C3X5LoQo130_provenance.
- NP202121.RAvqLfNsJgtUnFQDFQn1ex8Bb-_QvSD832dP9C3X5LoQo130_assertion wasGeneratedBy ECO_0000203 NP202121.RAvqLfNsJgtUnFQDFQn1ex8Bb-_QvSD832dP9C3X5LoQo130_provenance.