Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_assertion> ?p ?o ?g. }
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- NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_assertion type Assertion NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_head.
- NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_assertion wasGeneratedBy ECO_0000203 NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_provenance.
- NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_assertion wasDerivedFrom befree-20150227 NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_provenance.
- NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_assertion SIO_000772 19097999 NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_provenance.
- NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_assertion evidence source_evidence_literature NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_provenance.
- NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_assertion description "[Fragile X syndrome is a common inherited cause of mental retardation that results from loss or mutation of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_provenance.