@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0
> .
@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:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_head
{
this:
np:hasAssertion
dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_assertion
;
np:hasProvenance
dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_provenance
;
np:hasPublicationInfo
dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_assertion
a
np:Assertion
.
dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_provenance
a
np:Provenance
.
dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_assertion
{
miriam-gene:2332
a
ncit:C16612
.
lld:C0085215
a
ncit:C7057
.
dgn-gda:DGNcdb3d5289112b6e43ae309ed7cf007a5
sio:SIO_000628
miriam-gene:2332
,
lld:C0085215
;
a
sio:SIO_001122
.
}
dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_provenance
{
dgn-np:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_assertion
dcterms:description
"[The results of our research confirm the actuality of genetic tests of mutations in INHalpha1 and FMR1 genes among the women of reproductive age with the purpose of POF prognosis and prevention the birth of children with fragile X syndrome.]. 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:16161415
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP43902.RA83ctCIxQVtIMjYqzf3ttpAI1UFqbftTL2wSSGJ2Nwm0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}