@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP81685.RAY7pt2UyLxiYSgn_I0l9McOY7bbBc-_oYVQtByJDpNXI
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP81685.RAY7pt2UyLxiYSgn_I0l9McOY7bbBc-_oYVQtByJDpNXI130_head
{
this:
np:hasAssertion
dgn-np:NP81685.RAY7pt2UyLxiYSgn_I0l9McOY7bbBc-_oYVQtByJDpNXI130_assertion
;
np:hasProvenance
dgn-np:NP81685.RAY7pt2UyLxiYSgn_I0l9McOY7bbBc-_oYVQtByJDpNXI130_provenance
;
np:hasPublicationInfo
dgn-np:NP81685.RAY7pt2UyLxiYSgn_I0l9McOY7bbBc-_oYVQtByJDpNXI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP81685.RAY7pt2UyLxiYSgn_I0l9McOY7bbBc-_oYVQtByJDpNXI130_assertion
a
np:Assertion
.
dgn-np:NP81685.RAY7pt2UyLxiYSgn_I0l9McOY7bbBc-_oYVQtByJDpNXI130_provenance
a
np:Provenance
.
dgn-np:NP81685.RAY7pt2UyLxiYSgn_I0l9McOY7bbBc-_oYVQtByJDpNXI130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP81685.RAY7pt2UyLxiYSgn_I0l9McOY7bbBc-_oYVQtByJDpNXI130_assertion
{
miriam-gene:6470
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNf0f9407b2a3f68a0f8a86110ff6278fa
sio:SIO_000628
miriam-gene:6470
,
lld:C0004352
;
a
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.
}
dgn-np:NP81685.RAY7pt2UyLxiYSgn_I0l9McOY7bbBc-_oYVQtByJDpNXI130_provenance
{
dgn-np:NP81685.RAY7pt2UyLxiYSgn_I0l9McOY7bbBc-_oYVQtByJDpNXI130_assertion
dc:description
"[A total of 138 children diagnosed as autistic based on Diagnostic and Statistical Manual of Mental Disorders, fourth edition criteria and Autism Behavior Checklist scoring and 138 age and sex matched children who are nonautistic were tested for five genetic polymorphisms, that is, cytosolic serine hydroxyl methyl transferase (SHMT1 C1420T), methylene tetrahydrofolate reductase (MTHFR C677T and MTHFR A1298C), methionine synthase reductase (MTRR A66G), methionine synthase (MS A2756G) using PCR-restriction fragment length polymorphism methods.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:19440165
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP81685.RAY7pt2UyLxiYSgn_I0l9McOY7bbBc-_oYVQtByJDpNXI130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:40+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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