@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP252912.RAQbMgxL5W2i0lL8e-QIH_EsaFgah-5jMTG39UvYztTB4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP252912.RAQbMgxL5W2i0lL8e-QIH_EsaFgah-5jMTG39UvYztTB4130_head
{
this:
np:hasAssertion
dgn-np:NP252912.RAQbMgxL5W2i0lL8e-QIH_EsaFgah-5jMTG39UvYztTB4130_assertion
;
np:hasProvenance
dgn-np:NP252912.RAQbMgxL5W2i0lL8e-QIH_EsaFgah-5jMTG39UvYztTB4130_provenance
;
np:hasPublicationInfo
dgn-np:NP252912.RAQbMgxL5W2i0lL8e-QIH_EsaFgah-5jMTG39UvYztTB4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP252912.RAQbMgxL5W2i0lL8e-QIH_EsaFgah-5jMTG39UvYztTB4130_assertion
a
np:Assertion
.
dgn-np:NP252912.RAQbMgxL5W2i0lL8e-QIH_EsaFgah-5jMTG39UvYztTB4130_provenance
a
np:Provenance
.
dgn-np:NP252912.RAQbMgxL5W2i0lL8e-QIH_EsaFgah-5jMTG39UvYztTB4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP252912.RAQbMgxL5W2i0lL8e-QIH_EsaFgah-5jMTG39UvYztTB4130_assertion
{
miriam-gene:2332
a
ncit:C16612
.
lld:C0016667
a
ncit:C7057
.
dgn-gda:DGN217a2b0e17e3871a58cbaae80d3f77d5
sio:SIO_000628
miriam-gene:2332
,
lld:C0016667
;
a
sio:SIO_001121
.
}
dgn-np:NP252912.RAQbMgxL5W2i0lL8e-QIH_EsaFgah-5jMTG39UvYztTB4130_provenance
{
dgn-np:NP252912.RAQbMgxL5W2i0lL8e-QIH_EsaFgah-5jMTG39UvYztTB4130_assertion
dcterms:description
"[To test the hypothesis that absence of FMRP may affect the processing of specific transcripts, we have used an RNA differential display assay (RDDA) to identify differentially expressed transcripts in lymphoblast lines derived from fragile X syndrome patients.]. 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:10331605
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP252912.RAQbMgxL5W2i0lL8e-QIH_EsaFgah-5jMTG39UvYztTB4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:40+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}