@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP548793.RAwN30R-wFiVKo3lUBpvURdpgfi8mXJa8yw7w3O0bUWjI
> .
@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:NP548793.RAwN30R-wFiVKo3lUBpvURdpgfi8mXJa8yw7w3O0bUWjI130_head
{
this:
np:hasAssertion
dgn-np:NP548793.RAwN30R-wFiVKo3lUBpvURdpgfi8mXJa8yw7w3O0bUWjI130_assertion
;
np:hasProvenance
dgn-np:NP548793.RAwN30R-wFiVKo3lUBpvURdpgfi8mXJa8yw7w3O0bUWjI130_provenance
;
np:hasPublicationInfo
dgn-np:NP548793.RAwN30R-wFiVKo3lUBpvURdpgfi8mXJa8yw7w3O0bUWjI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP548793.RAwN30R-wFiVKo3lUBpvURdpgfi8mXJa8yw7w3O0bUWjI130_assertion
a
np:Assertion
.
dgn-np:NP548793.RAwN30R-wFiVKo3lUBpvURdpgfi8mXJa8yw7w3O0bUWjI130_provenance
a
np:Provenance
.
dgn-np:NP548793.RAwN30R-wFiVKo3lUBpvURdpgfi8mXJa8yw7w3O0bUWjI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP548793.RAwN30R-wFiVKo3lUBpvURdpgfi8mXJa8yw7w3O0bUWjI130_assertion
{
miriam-gene:2477
a
ncit:C16612
.
lld:C0037176
a
ncit:C7057
.
dgn-gda:DGN47fe372f0ffbcf89246eb435378ffe18
sio:SIO_000628
miriam-gene:2477
,
lld:C0037176
;
a
sio:SIO_001121
.
}
dgn-np:NP548793.RAwN30R-wFiVKo3lUBpvURdpgfi8mXJa8yw7w3O0bUWjI130_provenance
{
dgn-np:NP548793.RAwN30R-wFiVKo3lUBpvURdpgfi8mXJa8yw7w3O0bUWjI130_assertion
dcterms:description
"[Given that a single gene defect (FMR1) is known to be responsible for this disorder, we also assess whether brain activation in arithmetic processing areas is related to amount of FMR1 protein expression (FMRP).]. 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:12112763
;
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:NP548793.RAwN30R-wFiVKo3lUBpvURdpgfi8mXJa8yw7w3O0bUWjI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:31+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" .
}