@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP892576.RAEwgJ7SY3mY0BrouorhCwbZLgaptph_Q00S17Mkp0coI
> .
@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:NP892576.RAEwgJ7SY3mY0BrouorhCwbZLgaptph_Q00S17Mkp0coI130_head
{
this:
np:hasAssertion
dgn-np:NP892576.RAEwgJ7SY3mY0BrouorhCwbZLgaptph_Q00S17Mkp0coI130_assertion
;
np:hasProvenance
dgn-np:NP892576.RAEwgJ7SY3mY0BrouorhCwbZLgaptph_Q00S17Mkp0coI130_provenance
;
np:hasPublicationInfo
dgn-np:NP892576.RAEwgJ7SY3mY0BrouorhCwbZLgaptph_Q00S17Mkp0coI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP892576.RAEwgJ7SY3mY0BrouorhCwbZLgaptph_Q00S17Mkp0coI130_assertion
a
np:Assertion
.
dgn-np:NP892576.RAEwgJ7SY3mY0BrouorhCwbZLgaptph_Q00S17Mkp0coI130_provenance
a
np:Provenance
.
dgn-np:NP892576.RAEwgJ7SY3mY0BrouorhCwbZLgaptph_Q00S17Mkp0coI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP892576.RAEwgJ7SY3mY0BrouorhCwbZLgaptph_Q00S17Mkp0coI130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0020255
a
ncit:C7057
.
dgn-gda:DGN4a6b31f76ca68e1f711cee863867cd64
sio:SIO_000628
miriam-gene:3126
,
lld:C0020255
;
a
sio:SIO_001121
.
}
dgn-np:NP892576.RAEwgJ7SY3mY0BrouorhCwbZLgaptph_Q00S17Mkp0coI130_provenance
{
dgn-np:NP892576.RAEwgJ7SY3mY0BrouorhCwbZLgaptph_Q00S17Mkp0coI130_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:NP892576.RAEwgJ7SY3mY0BrouorhCwbZLgaptph_Q00S17Mkp0coI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:08+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" .
}