@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP720918.RANpsvRS-fS-5aEFvjxdKL7XjecrhVHAY4XqbvnJ8GwII
> .
@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:NP720918.RANpsvRS-fS-5aEFvjxdKL7XjecrhVHAY4XqbvnJ8GwII130_head
{
this:
np:hasAssertion
dgn-np:NP720918.RANpsvRS-fS-5aEFvjxdKL7XjecrhVHAY4XqbvnJ8GwII130_assertion
;
np:hasProvenance
dgn-np:NP720918.RANpsvRS-fS-5aEFvjxdKL7XjecrhVHAY4XqbvnJ8GwII130_provenance
;
np:hasPublicationInfo
dgn-np:NP720918.RANpsvRS-fS-5aEFvjxdKL7XjecrhVHAY4XqbvnJ8GwII130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP720918.RANpsvRS-fS-5aEFvjxdKL7XjecrhVHAY4XqbvnJ8GwII130_assertion
a
np:Assertion
.
dgn-np:NP720918.RANpsvRS-fS-5aEFvjxdKL7XjecrhVHAY4XqbvnJ8GwII130_provenance
a
np:Provenance
.
dgn-np:NP720918.RANpsvRS-fS-5aEFvjxdKL7XjecrhVHAY4XqbvnJ8GwII130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP720918.RANpsvRS-fS-5aEFvjxdKL7XjecrhVHAY4XqbvnJ8GwII130_assertion
{
miriam-gene:2332
a
ncit:C16612
.
lld:C0154208
a
ncit:C7057
.
dgn-gda:DGN6745c2b93d5d29c06c3236bb48854723
sio:SIO_000628
miriam-gene:2332
,
lld:C0154208
;
a
sio:SIO_001121
.
}
dgn-np:NP720918.RANpsvRS-fS-5aEFvjxdKL7XjecrhVHAY4XqbvnJ8GwII130_provenance
{
dgn-np:NP720918.RANpsvRS-fS-5aEFvjxdKL7XjecrhVHAY4XqbvnJ8GwII130_assertion
dcterms:description
"[The association between FMR1 premutation and ovarian dysfunction has been widely studied, and many factors such as the repeat tract size, the sequence organization of the CGG repeat tract, the parental origin of the premutation, and the FMR1 mRNA levels have been examined.]. 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:19373114
;
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:NP720918.RANpsvRS-fS-5aEFvjxdKL7XjecrhVHAY4XqbvnJ8GwII130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:18+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" .
}