@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP805008.RAQkStFqhZoN7qDnXl3mQNrInodsL5ZINnt4S5C4hWpyc
> .
@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 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#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP805008.RAQkStFqhZoN7qDnXl3mQNrInodsL5ZINnt4S5C4hWpyc130_head
{
this:
np:hasAssertion
dgn-np:NP805008.RAQkStFqhZoN7qDnXl3mQNrInodsL5ZINnt4S5C4hWpyc130_assertion
;
np:hasProvenance
dgn-np:NP805008.RAQkStFqhZoN7qDnXl3mQNrInodsL5ZINnt4S5C4hWpyc130_provenance
;
np:hasPublicationInfo
dgn-np:NP805008.RAQkStFqhZoN7qDnXl3mQNrInodsL5ZINnt4S5C4hWpyc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP805008.RAQkStFqhZoN7qDnXl3mQNrInodsL5ZINnt4S5C4hWpyc130_assertion
a
np:Assertion
.
dgn-np:NP805008.RAQkStFqhZoN7qDnXl3mQNrInodsL5ZINnt4S5C4hWpyc130_provenance
a
np:Provenance
.
dgn-np:NP805008.RAQkStFqhZoN7qDnXl3mQNrInodsL5ZINnt4S5C4hWpyc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP805008.RAQkStFqhZoN7qDnXl3mQNrInodsL5ZINnt4S5C4hWpyc130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0040560
a
ncit:C7057
.
dgn-gda:DGN53704e4380a30f3e2c20c0a550032fb0
sio:SIO_000628
miriam-gene:3126
,
lld:C0040560
;
a
sio:SIO_001121
.
}
dgn-np:NP805008.RAQkStFqhZoN7qDnXl3mQNrInodsL5ZINnt4S5C4hWpyc130_provenance
{
dgn-np:NP805008.RAQkStFqhZoN7qDnXl3mQNrInodsL5ZINnt4S5C4hWpyc130_assertion
dcterms:description
"[We characterized effects of HLA-DQ alleles on outcome of congenital toxoplasma infection and found that among Caucasians, the DQ3 gene frequency was significantly higher in infected infants with hydrocephalus (0.783) than infected infants without hydrocephalus (0.444) or published normal controls (0.487).]. 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:10579423
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
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 .
}
dgn-np:NP805008.RAQkStFqhZoN7qDnXl3mQNrInodsL5ZINnt4S5C4hWpyc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:13+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}