PubMed:18773291
Annnotations
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T1 | 0-50 | Sentence | denotes | Dystroglycan glycosylation and muscular dystrophy. |
TextSentencer_T2 | 51-205 | Sentence | denotes | Dystroglycan is an integral member of the skeletal muscle dystrophin glycoprotein complex, which links dystrophin to proteins in the extracellular matrix. |
TextSentencer_T3 | 206-358 | Sentence | denotes | Recently, a group of human muscular dystrophy disorders have been demonstrated to result from defective glycosylation of the alpha-dystroglycan subunit. |
TextSentencer_T4 | 359-520 | Sentence | denotes | Genetic studies of these diseases have identified six genes that encode proteins required for the synthesis of essential carbohydrate structures on dystroglycan. |
TextSentencer_T5 | 521-575 | Sentence | denotes | Here we highlight their known or postulated functions. |
TextSentencer_T6 | 576-734 | Sentence | denotes | This glycosylation pathway appears to be highly specific (dystroglycan is the only substrate identified thus far) and to be highly conserved during evolution. |
T1 | 0-50 | Sentence | denotes | Dystroglycan glycosylation and muscular dystrophy. |
T2 | 51-205 | Sentence | denotes | Dystroglycan is an integral member of the skeletal muscle dystrophin glycoprotein complex, which links dystrophin to proteins in the extracellular matrix. |
T3 | 206-358 | Sentence | denotes | Recently, a group of human muscular dystrophy disorders have been demonstrated to result from defective glycosylation of the alpha-dystroglycan subunit. |
T4 | 359-520 | Sentence | denotes | Genetic studies of these diseases have identified six genes that encode proteins required for the synthesis of essential carbohydrate structures on dystroglycan. |
T5 | 521-575 | Sentence | denotes | Here we highlight their known or postulated functions. |
T6 | 576-734 | Sentence | denotes | This glycosylation pathway appears to be highly specific (dystroglycan is the only substrate identified thus far) and to be highly conserved during evolution. |
Glycosmos6-MAT
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 93-108 | http://purl.obolibrary.org/obo/MAT_0000302 | denotes | skeletal muscle |
T2 | 102-108 | http://purl.obolibrary.org/obo/MAT_0000025 | denotes | muscle |
DisGeNET
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T0 | 0-12 | gene:1605 | denotes | Dystroglycan |
T1 | 31-49 | disease:C0026850 | denotes | muscular dystrophy |
R1 | T0 | T1 | associated_with | Dystroglycan,muscular dystrophy |
DisGeNET5_gene_disease
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
18773291-0#0#12#gene1605 | 51-63 | gene1605 | denotes | Dystroglycan |
18773291-0#31#49#diseaseC0026850 | 298-584 | diseaseC0026850 | denotes | m defective glycosylation of the alpha-dystroglycan subunit. Genetic studies of these diseases have identified six genes that encode proteins required for the synthesis of essential carbohydrate structures on dystroglycan. Here we highlight their known or postulated functions. This gly |
0#12#gene160531#49#diseaseC0026850 | 18773291-0#0#12#gene1605 | 18773291-0#31#49#diseaseC0026850 | associated_with | Dystroglycan,m defective glycosylation of the alpha-dystroglycan subunit. Genetic studies of these diseases have identified six genes that encode proteins required for the synthesis of essential carbohydrate structures on dystroglycan. Here we highlight their known or postulated functions. This gly |
Anatomy-MAT
Id | Subject | Object | Predicate | Lexical cue | mat_id |
---|---|---|---|---|---|
T1 | 93-108 | Body_part | denotes | skeletal muscle | http://purl.obolibrary.org/obo/MAT_0000302 |
HP-phenotype
Id | Subject | Object | Predicate | Lexical cue | hp_id |
---|---|---|---|---|---|
T1 | 31-49 | Phenotype | denotes | muscular dystrophy | HP:0003560 |
T2 | 233-251 | Phenotype | denotes | muscular dystrophy | HP:0003560 |
mondo_disease
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 31-49 | Disease | denotes | muscular dystrophy | http://purl.obolibrary.org/obo/MONDO_0020121 |
T2 | 233-251 | Disease | denotes | muscular dystrophy | http://purl.obolibrary.org/obo/MONDO_0020121 |
NCBITAXON
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T1 | 227-232 | OrganismTaxon | denotes | human | 9606 |
Anatomy-UBERON
Id | Subject | Object | Predicate | Lexical cue | uberon_id |
---|---|---|---|---|---|
T1 | 93-108 | Body_part | denotes | skeletal muscle | http://purl.obolibrary.org/obo/UBERON_0001134|http://purl.obolibrary.org/obo/UBERON_0014892|http://purl.obolibrary.org/obo/UBERON_0014895 |
T4 | 184-204 | Body_part | denotes | extracellular matrix | http://purl.obolibrary.org/obo/GO_0031012 |