@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP184894.RAjEkwvLsv4Egz8Qmst49VEESoQ3Vcq8B5_Sysv5q5km0
> .
@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:NP184894.RAjEkwvLsv4Egz8Qmst49VEESoQ3Vcq8B5_Sysv5q5km0130_head
{
this:
np:hasAssertion
dgn-np:NP184894.RAjEkwvLsv4Egz8Qmst49VEESoQ3Vcq8B5_Sysv5q5km0130_assertion
;
np:hasProvenance
dgn-np:NP184894.RAjEkwvLsv4Egz8Qmst49VEESoQ3Vcq8B5_Sysv5q5km0130_provenance
;
np:hasPublicationInfo
dgn-np:NP184894.RAjEkwvLsv4Egz8Qmst49VEESoQ3Vcq8B5_Sysv5q5km0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP184894.RAjEkwvLsv4Egz8Qmst49VEESoQ3Vcq8B5_Sysv5q5km0130_assertion
a
np:Assertion
.
dgn-np:NP184894.RAjEkwvLsv4Egz8Qmst49VEESoQ3Vcq8B5_Sysv5q5km0130_provenance
a
np:Provenance
.
dgn-np:NP184894.RAjEkwvLsv4Egz8Qmst49VEESoQ3Vcq8B5_Sysv5q5km0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP184894.RAjEkwvLsv4Egz8Qmst49VEESoQ3Vcq8B5_Sysv5q5km0130_assertion
{
miriam-gene:5625
a
ncit:C16612
.
lld:C0033975
a
ncit:C7057
.
dgn-gda:DGNdfbe7a903ef0757ebedde8a1bad91962
sio:SIO_000628
miriam-gene:5625
,
lld:C0033975
;
a
sio:SIO_001121
.
}
dgn-np:NP184894.RAjEkwvLsv4Egz8Qmst49VEESoQ3Vcq8B5_Sysv5q5km0130_provenance
{
dgn-np:NP184894.RAjEkwvLsv4Egz8Qmst49VEESoQ3Vcq8B5_Sysv5q5km0130_assertion
dcterms:description
"[We did not detect 22q11 interstitial deletions associated with the DiGeorge syndrome among the 320 patients of our sample and we found no association between common PRODH polymorphisms and any of the psychotic disorders.]. 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:15494707
;
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:NP184894.RAjEkwvLsv4Egz8Qmst49VEESoQ3Vcq8B5_Sysv5q5km0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:41+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" .
}