@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP629049.RAc7h6sE8FBSoR-IEKjqv5bTyzd7fP8gf5getl4CECrFs
> .
@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:NP629049.RAc7h6sE8FBSoR-IEKjqv5bTyzd7fP8gf5getl4CECrFs130_head
{
this:
np:hasAssertion
dgn-np:NP629049.RAc7h6sE8FBSoR-IEKjqv5bTyzd7fP8gf5getl4CECrFs130_assertion
;
np:hasProvenance
dgn-np:NP629049.RAc7h6sE8FBSoR-IEKjqv5bTyzd7fP8gf5getl4CECrFs130_provenance
;
np:hasPublicationInfo
dgn-np:NP629049.RAc7h6sE8FBSoR-IEKjqv5bTyzd7fP8gf5getl4CECrFs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP629049.RAc7h6sE8FBSoR-IEKjqv5bTyzd7fP8gf5getl4CECrFs130_assertion
a
np:Assertion
.
dgn-np:NP629049.RAc7h6sE8FBSoR-IEKjqv5bTyzd7fP8gf5getl4CECrFs130_provenance
a
np:Provenance
.
dgn-np:NP629049.RAc7h6sE8FBSoR-IEKjqv5bTyzd7fP8gf5getl4CECrFs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP629049.RAc7h6sE8FBSoR-IEKjqv5bTyzd7fP8gf5getl4CECrFs130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0012236
a
ncit:C7057
.
dgn-gda:DGN3229b0534d781ffcfda41b9fba086dd1
sio:SIO_000628
miriam-gene:1312
,
lld:C0012236
;
a
sio:SIO_001121
.
}
dgn-np:NP629049.RAc7h6sE8FBSoR-IEKjqv5bTyzd7fP8gf5getl4CECrFs130_provenance
{
dgn-np:NP629049.RAc7h6sE8FBSoR-IEKjqv5bTyzd7fP8gf5getl4CECrFs130_assertion
dcterms:description
"[We hypothesized an interaction between the COMT(158) genotype and proline, predicting the strongest negative effect of high proline on brain function to occur in 22q11DS children who are carriers of the COMT(met) allele.]. 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:18769474
;
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:NP629049.RAc7h6sE8FBSoR-IEKjqv5bTyzd7fP8gf5getl4CECrFs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:19+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" .
}