PubMed:23514716 / 1513-1713 JSONTXT

Annnotations TAB JSON ListView MergeView

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T15 0-200 Sentence denotes These experiments demonstrate that loss of mouse Cmah can worsen disease severity in more than one form of muscular dystrophy and suggest that Cmah may be a general genetic modifier of muscle disease.
T13 0-200 Sentence denotes These experiments demonstrate that loss of mouse Cmah can worsen disease severity in more than one form of muscular dystrophy and suggest that Cmah may be a general genetic modifier of muscle disease.
T15 0-200 Sentence denotes These experiments demonstrate that loss of mouse Cmah can worsen disease severity in more than one form of muscular dystrophy and suggest that Cmah may be a general genetic modifier of muscle disease.

Glycosmos6-MAT

Id Subject Object Predicate Lexical cue
T8 185-191 http://purl.obolibrary.org/obo/MAT_0000025 denotes muscle

ICD10

Id Subject Object Predicate Lexical cue
T5 107-125 http://purl.bioontology.org/ontology/ICD10/G71.0 denotes muscular dystrophy

GlycoBiology-FMA

Id Subject Object Predicate Lexical cue
_T56 116-125 FMAID:62357 denotes dystrophy
_T57 116-125 FMAID:165876 denotes dystrophy
_T58 185-191 FMAID:172175 denotes muscle
_T59 185-191 FMAID:123535 denotes muscle
_T60 185-191 FMAID:30316 denotes muscle

uniprot-mouse

Id Subject Object Predicate Lexical cue
T10 49-53 http://www.uniprot.org/uniprot/Q61419 denotes Cmah
T11 143-147 http://www.uniprot.org/uniprot/Q61419 denotes Cmah

EDAM-topics

Id Subject Object Predicate Lexical cue
T13 65-72 http://edamontology.org/topic_0634 denotes disease
T14 165-172 http://edamontology.org/topic_3053 denotes genetic
T15 192-199 http://edamontology.org/topic_0634 denotes disease

EDAM-DFO

Id Subject Object Predicate Lexical cue
T4 18-29 http://edamontology.org/operation_2246 denotes demonstrate
T5 157-164 http://edamontology.org/operation_3429 denotes general

PubmedHPO

Id Subject Object Predicate Lexical cue
T6 107-125 HP_0003560 denotes muscular dystrophy

GlycoBiology-MAT

Id Subject Object Predicate Lexical cue
T8 185-191 http://purl.obolibrary.org/obo/MAT_0000025 denotes muscle

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T5 107-125 Disease denotes muscular dystrophy http://purl.obolibrary.org/obo/MONDO_0020121

Anatomy-MAT

Id Subject Object Predicate Lexical cue mat_id
T5 185-191 Body_part denotes muscle http://purl.obolibrary.org/obo/MAT_0000025

GlyCosmos15-HP

Id Subject Object Predicate Lexical cue hp_id
T5 107-125 Phenotype denotes muscular dystrophy HP:0003560

GlyCosmos15-MONDO

Id Subject Object Predicate Lexical cue mondo_id
T5 107-125 Disease denotes muscular dystrophy http://purl.obolibrary.org/obo/MONDO_0020121

GlyCosmos15-NCBITAXON

Id Subject Object Predicate Lexical cue db_id
T15 43-48 OrganismTaxon denotes mouse 10088|10090

GlyCosmos15-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T12 185-191 Body_part denotes muscle http://purl.obolibrary.org/obo/UBERON_0001630|http://purl.obolibrary.org/obo/UBERON_0005090

GlyCosmos15-MAT

Id Subject Object Predicate Lexical cue mat_id
T5 185-191 Body_part denotes muscle http://purl.obolibrary.org/obo/MAT_0000025

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T15 0-200 Sentence denotes These experiments demonstrate that loss of mouse Cmah can worsen disease severity in more than one form of muscular dystrophy and suggest that Cmah may be a general genetic modifier of muscle disease.
T13 0-200 Sentence denotes These experiments demonstrate that loss of mouse Cmah can worsen disease severity in more than one form of muscular dystrophy and suggest that Cmah may be a general genetic modifier of muscle disease.
T15 0-200 Sentence denotes These experiments demonstrate that loss of mouse Cmah can worsen disease severity in more than one form of muscular dystrophy and suggest that Cmah may be a general genetic modifier of muscle disease.

GlyCosmos15-Sentences

Id Subject Object Predicate Lexical cue
T13 0-200 Sentence denotes These experiments demonstrate that loss of mouse Cmah can worsen disease severity in more than one form of muscular dystrophy and suggest that Cmah may be a general genetic modifier of muscle disease.

NCBITAXON

Id Subject Object Predicate Lexical cue db_id
T15 43-48 OrganismTaxon denotes mouse 10088|10090

Anatomy-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T12 185-191 Body_part denotes muscle http://purl.obolibrary.org/obo/UBERON_0001630|http://purl.obolibrary.org/obo/UBERON_0005090

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T5 107-125 Phenotype denotes muscular dystrophy HP:0003560