@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP783663.RAWbX_OF_3mM0f_Swzja9xJMy-1m2ExfR5gpoGHia12BU
> .
@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:NP783663.RAWbX_OF_3mM0f_Swzja9xJMy-1m2ExfR5gpoGHia12BU130_head
{
this:
np:hasAssertion
dgn-np:NP783663.RAWbX_OF_3mM0f_Swzja9xJMy-1m2ExfR5gpoGHia12BU130_assertion
;
np:hasProvenance
dgn-np:NP783663.RAWbX_OF_3mM0f_Swzja9xJMy-1m2ExfR5gpoGHia12BU130_provenance
;
np:hasPublicationInfo
dgn-np:NP783663.RAWbX_OF_3mM0f_Swzja9xJMy-1m2ExfR5gpoGHia12BU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP783663.RAWbX_OF_3mM0f_Swzja9xJMy-1m2ExfR5gpoGHia12BU130_assertion
a
np:Assertion
.
dgn-np:NP783663.RAWbX_OF_3mM0f_Swzja9xJMy-1m2ExfR5gpoGHia12BU130_provenance
a
np:Provenance
.
dgn-np:NP783663.RAWbX_OF_3mM0f_Swzja9xJMy-1m2ExfR5gpoGHia12BU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP783663.RAWbX_OF_3mM0f_Swzja9xJMy-1m2ExfR5gpoGHia12BU130_assertion
{
miriam-gene:5625
a
ncit:C16612
.
lld:C0012236
a
ncit:C7057
.
dgn-gda:DGN1a91877633932b20e2d69478f5cfcfef
sio:SIO_000628
miriam-gene:5625
,
lld:C0012236
;
a
sio:SIO_001121
.
}
dgn-np:NP783663.RAWbX_OF_3mM0f_Swzja9xJMy-1m2ExfR5gpoGHia12BU130_provenance
{
dgn-np:NP783663.RAWbX_OF_3mM0f_Swzja9xJMy-1m2ExfR5gpoGHia12BU130_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:NP783663.RAWbX_OF_3mM0f_Swzja9xJMy-1m2ExfR5gpoGHia12BU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:54+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" .
}