Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_provenance.
- befree-2016 importedOn "2016-02-19" NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_provenance.
- NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_assertion wasGeneratedBy ECO_0000203 NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_provenance.
- NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_assertion wasDerivedFrom befree-2016 NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_provenance.
- NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_assertion SIO_000772 19097999 NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_provenance.
- NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_assertion evidence source_evidence_literature NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_provenance.
- NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_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." NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_provenance.