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PubMed:6517102 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-57 Sentence denotes Hyperpipecolic acidemia in neonatal adrenoleukodystrophy.
TextSentencer_T2 58-212 Sentence denotes Serum pipecolic acid was measured in patients with neonatal adrenoleukodystrophy (NALD), sex-linked ALD, and the cerebrohepatorenal syndrome of Zellweger.
TextSentencer_T3 213-455 Sentence denotes Pipecolic acid was elevated, often markedly, in most of the patients with NALD but in none of those with X-linked ALD or adrenomyeloneuropathy, or in normal adults and children, or children with cirrhosis or other neurodegenerative disorders.
TextSentencer_T4 456-804 Sentence denotes The demonstration of elevated serum pipecolic acid in NALD adds to the previously recognized elevation of very-long-chain fatty acids (another Zellweger syndrome sign) and suggests that generalized peroxisomal dysfunction may be a characteristic of NALD as it appears to be of Zellweger syndrome, which diseases share some clinical characteristics.
TextSentencer_T5 805-863 Sentence denotes The nosologic significance of these findings is discussed.
T1 0-57 Sentence denotes Hyperpipecolic acidemia in neonatal adrenoleukodystrophy.
T2 58-212 Sentence denotes Serum pipecolic acid was measured in patients with neonatal adrenoleukodystrophy (NALD), sex-linked ALD, and the cerebrohepatorenal syndrome of Zellweger.
T3 213-455 Sentence denotes Pipecolic acid was elevated, often markedly, in most of the patients with NALD but in none of those with X-linked ALD or adrenomyeloneuropathy, or in normal adults and children, or children with cirrhosis or other neurodegenerative disorders.
T4 456-804 Sentence denotes The demonstration of elevated serum pipecolic acid in NALD adds to the previously recognized elevation of very-long-chain fatty acids (another Zellweger syndrome sign) and suggests that generalized peroxisomal dysfunction may be a characteristic of NALD as it appears to be of Zellweger syndrome, which diseases share some clinical characteristics.
T5 805-863 Sentence denotes The nosologic significance of these findings is discussed.

DisGeNET

Id Subject Object Predicate Lexical cue
T0 158-161 gene:215 denotes ALD
T1 109-138 disease:C0282525 denotes neonatal adrenoleukodystrophy
T2 158-161 gene:215 denotes ALD
T3 171-198 disease:C0043459 denotes cerebrohepatorenal syndrome
T4 327-330 gene:215 denotes ALD
T5 334-355 disease:C0162309 denotes adrenomyeloneuropathy
T6 327-330 gene:215 denotes ALD
T7 334-355 disease:C1527231 denotes adrenomyeloneuropathy
R1 T0 T1 associated_with ALD,neonatal adrenoleukodystrophy
R2 T2 T3 associated_with ALD,cerebrohepatorenal syndrome
R3 T4 T5 associated_with ALD,adrenomyeloneuropathy
R4 T6 T7 associated_with ALD,adrenomyeloneuropathy

DisGeNet-2017-sample

Id Subject Object Predicate Lexical cue
T949 327-330 gene:215 denotes ALD
T950 334-355 disease:C0162309 denotes adrenomyeloneuropathy
R1 T949 T950 associated_with ALD,adrenomyeloneuropathy
R2 T949 T950 associated_with ALD,adrenomyeloneuropathy

UBERON-AE

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 486-491 http://purl.obolibrary.org/obo/UBERON_0001977 denotes serum

performance-test

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 58-63 http://purl.obolibrary.org/obo/UBERON_0001977 denotes Serum
PD-UBERON-AE-B_T2 486-491 http://purl.obolibrary.org/obo/UBERON_0001977 denotes serum