@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP176878.RAJdGwFZeDW57tD6DwcvYCeTw82Dqc_v-C83FPJjQn0dM
> .
@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:NP176878.RAJdGwFZeDW57tD6DwcvYCeTw82Dqc_v-C83FPJjQn0dM130_head
{
this:
np:hasAssertion
dgn-np:NP176878.RAJdGwFZeDW57tD6DwcvYCeTw82Dqc_v-C83FPJjQn0dM130_assertion
;
np:hasProvenance
dgn-np:NP176878.RAJdGwFZeDW57tD6DwcvYCeTw82Dqc_v-C83FPJjQn0dM130_provenance
;
np:hasPublicationInfo
dgn-np:NP176878.RAJdGwFZeDW57tD6DwcvYCeTw82Dqc_v-C83FPJjQn0dM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP176878.RAJdGwFZeDW57tD6DwcvYCeTw82Dqc_v-C83FPJjQn0dM130_assertion
a
np:Assertion
.
dgn-np:NP176878.RAJdGwFZeDW57tD6DwcvYCeTw82Dqc_v-C83FPJjQn0dM130_provenance
a
np:Provenance
.
dgn-np:NP176878.RAJdGwFZeDW57tD6DwcvYCeTw82Dqc_v-C83FPJjQn0dM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP176878.RAJdGwFZeDW57tD6DwcvYCeTw82Dqc_v-C83FPJjQn0dM130_assertion
{
miriam-gene:2332
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGN1389c06cd6c6de2edd1c6baf646fdcc0
sio:SIO_000628
miriam-gene:2332
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP176878.RAJdGwFZeDW57tD6DwcvYCeTw82Dqc_v-C83FPJjQn0dM130_provenance
{
dgn-np:NP176878.RAJdGwFZeDW57tD6DwcvYCeTw82Dqc_v-C83FPJjQn0dM130_assertion
dcterms:description
"[Polymerase chain reaction (PCR) technique combined with direct detection by silver staining on denaturing DNA sequencing gel was used to analyze the (CGG)n repeats within the FMR1 gene on 169 suspected patients with mental retardation and 33 kindreds of 6 fragile X families.]. 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:12840860
;
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:NP176878.RAJdGwFZeDW57tD6DwcvYCeTw82Dqc_v-C83FPJjQn0dM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:35+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" .
}