PubMed:16158428 JSONTXT 25 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue #label
T1 54-59 GeneOrGeneProduct denotes OPHN1
T2 200-205 GeneOrGeneProduct denotes OPHN1
T3 256-268 GeneOrGeneProduct denotes non-specific
T36129 269-287 DiseaseOrPhenotypicFeature denotes mental retardation D008607
T10077 320-325 OrganismTaxon denotes fossa
T89335 331-352 DiseaseOrPhenotypicFeature denotes cerebellar hypoplasia C562568
T66723 388-396 OrganismTaxon denotes patients
T5680 448-475 DiseaseOrPhenotypicFeature denotes X-linked mental retardation D038901
T4 495-500 GeneOrGeneProduct denotes OPHN1
T40044 683-704 DiseaseOrPhenotypicFeature denotes cerebellar hypoplasia C562568
T5 853-871 DiseaseOrPhenotypicFeature denotes mental retardation D008607