Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_provenance.
- 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.