@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP401383.RAZ38s0Ve9UBNSfNFKMx0GJYdQdQ2t9erQfjm8AKKzKGE
> .
@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:NP401383.RAZ38s0Ve9UBNSfNFKMx0GJYdQdQ2t9erQfjm8AKKzKGE130_head
{
this:
np:hasAssertion
dgn-np:NP401383.RAZ38s0Ve9UBNSfNFKMx0GJYdQdQ2t9erQfjm8AKKzKGE130_assertion
;
np:hasProvenance
dgn-np:NP401383.RAZ38s0Ve9UBNSfNFKMx0GJYdQdQ2t9erQfjm8AKKzKGE130_provenance
;
np:hasPublicationInfo
dgn-np:NP401383.RAZ38s0Ve9UBNSfNFKMx0GJYdQdQ2t9erQfjm8AKKzKGE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP401383.RAZ38s0Ve9UBNSfNFKMx0GJYdQdQ2t9erQfjm8AKKzKGE130_assertion
a
np:Assertion
.
dgn-np:NP401383.RAZ38s0Ve9UBNSfNFKMx0GJYdQdQ2t9erQfjm8AKKzKGE130_provenance
a
np:Provenance
.
dgn-np:NP401383.RAZ38s0Ve9UBNSfNFKMx0GJYdQdQ2t9erQfjm8AKKzKGE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP401383.RAZ38s0Ve9UBNSfNFKMx0GJYdQdQ2t9erQfjm8AKKzKGE130_assertion
{
miriam-gene:2332
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGNafb4d5979def4df3b7fe2b9114e659e5
sio:SIO_000628
miriam-gene:2332
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP401383.RAZ38s0Ve9UBNSfNFKMx0GJYdQdQ2t9erQfjm8AKKzKGE130_provenance
{
dgn-np:NP401383.RAZ38s0Ve9UBNSfNFKMx0GJYdQdQ2t9erQfjm8AKKzKGE130_assertion
dcterms:description
"[Immunocytochemistry showed FMRP expression in regions of the brain with the unmethylated mutation (superior temporal cortex, frontal cortex, and hippocampus) and no expression in the region with the methylated full mutation (parietal).]. 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:10331599
;
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:NP401383.RAZ38s0Ve9UBNSfNFKMx0GJYdQdQ2t9erQfjm8AKKzKGE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:59+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" .
}