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http://rdf.disgenet.org/nanopublications.trig#NP807025.RAjRsnlllEUHhKf3MTseMtBlcSsiqSefg159ny0Yzv0oU
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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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 dcterms: <
http://purl.org/dc/terms/
> .
@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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP807025.RAjRsnlllEUHhKf3MTseMtBlcSsiqSefg159ny0Yzv0oU130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP807025.RAjRsnlllEUHhKf3MTseMtBlcSsiqSefg159ny0Yzv0oU130_assertion
a
np:Assertion
.
dgn-np:NP807025.RAjRsnlllEUHhKf3MTseMtBlcSsiqSefg159ny0Yzv0oU130_provenance
a
np:Provenance
.
dgn-np:NP807025.RAjRsnlllEUHhKf3MTseMtBlcSsiqSefg159ny0Yzv0oU130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:8170
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN6fea01823f97d3dec787116601705cd1
sio:SIO_000628
miriam-gene:8170
,
lld:C0004352
;
a
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.
}
dgn-np:NP807025.RAjRsnlllEUHhKf3MTseMtBlcSsiqSefg159ny0Yzv0oU130_provenance
{
dgn-np:NP807025.RAjRsnlllEUHhKf3MTseMtBlcSsiqSefg159ny0Yzv0oU130_assertion
dcterms:description
"[We genotyped all four WNT2 polymorphisms and a polymorphic trinucleotide repeat in the 5' UTR of RELN in 107 families with multiple autistic children, and evaluated evidence for association between these variants and autism by the transmission disequilibrium test (TDT).]. 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:15048648
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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 .
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dgn-np:NP807025.RAjRsnlllEUHhKf3MTseMtBlcSsiqSefg159ny0Yzv0oU130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
<
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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pav:version
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