@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP587798.RA6ki6fl98h73A8KTQNjeYSHj3eNUOwsQdiHx4zKCYIdo
> .
@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:NP587798.RA6ki6fl98h73A8KTQNjeYSHj3eNUOwsQdiHx4zKCYIdo130_head
{
this:
np:hasAssertion
dgn-np:NP587798.RA6ki6fl98h73A8KTQNjeYSHj3eNUOwsQdiHx4zKCYIdo130_assertion
;
np:hasProvenance
dgn-np:NP587798.RA6ki6fl98h73A8KTQNjeYSHj3eNUOwsQdiHx4zKCYIdo130_provenance
;
np:hasPublicationInfo
dgn-np:NP587798.RA6ki6fl98h73A8KTQNjeYSHj3eNUOwsQdiHx4zKCYIdo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP587798.RA6ki6fl98h73A8KTQNjeYSHj3eNUOwsQdiHx4zKCYIdo130_assertion
a
np:Assertion
.
dgn-np:NP587798.RA6ki6fl98h73A8KTQNjeYSHj3eNUOwsQdiHx4zKCYIdo130_provenance
a
np:Provenance
.
dgn-np:NP587798.RA6ki6fl98h73A8KTQNjeYSHj3eNUOwsQdiHx4zKCYIdo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP587798.RA6ki6fl98h73A8KTQNjeYSHj3eNUOwsQdiHx4zKCYIdo130_assertion
{
miriam-gene:24
a
ncit:C16612
.
lld:C0275544
a
ncit:C7057
.
dgn-gda:DGN4fdaf5c4451ff46fb76e323cc181f99f
sio:SIO_000628
miriam-gene:24
,
lld:C0275544
;
a
sio:SIO_001121
.
}
dgn-np:NP587798.RA6ki6fl98h73A8KTQNjeYSHj3eNUOwsQdiHx4zKCYIdo130_provenance
{
dgn-np:NP587798.RA6ki6fl98h73A8KTQNjeYSHj3eNUOwsQdiHx4zKCYIdo130_assertion
dcterms:description
"[These associations between clinical outcomes of congenital toxoplasmosis and polymorphisms at ABCA4 and COL2A1 provide novel insight into the molecular pathways that can be affected by congenital infection with this parasite.]. 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:18523590
;
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:NP587798.RA6ki6fl98h73A8KTQNjeYSHj3eNUOwsQdiHx4zKCYIdo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}