@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP755048.RAFbsZ27_ctYzOZU00-mzNRmfALWJfQJzWiNxpNZLuMb4
> .
@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:NP755048.RAFbsZ27_ctYzOZU00-mzNRmfALWJfQJzWiNxpNZLuMb4130_head
{
this:
np:hasAssertion
dgn-np:NP755048.RAFbsZ27_ctYzOZU00-mzNRmfALWJfQJzWiNxpNZLuMb4130_assertion
;
np:hasProvenance
dgn-np:NP755048.RAFbsZ27_ctYzOZU00-mzNRmfALWJfQJzWiNxpNZLuMb4130_provenance
;
np:hasPublicationInfo
dgn-np:NP755048.RAFbsZ27_ctYzOZU00-mzNRmfALWJfQJzWiNxpNZLuMb4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP755048.RAFbsZ27_ctYzOZU00-mzNRmfALWJfQJzWiNxpNZLuMb4130_assertion
a
np:Assertion
.
dgn-np:NP755048.RAFbsZ27_ctYzOZU00-mzNRmfALWJfQJzWiNxpNZLuMb4130_provenance
a
np:Provenance
.
dgn-np:NP755048.RAFbsZ27_ctYzOZU00-mzNRmfALWJfQJzWiNxpNZLuMb4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP755048.RAFbsZ27_ctYzOZU00-mzNRmfALWJfQJzWiNxpNZLuMb4130_assertion
{
miriam-gene:2263
a
ncit:C16612
.
lld:C0032897
a
ncit:C7057
.
dgn-gda:DGN47f3411397824ae860799c114d01e44f
sio:SIO_000628
miriam-gene:2263
,
lld:C0032897
;
a
sio:SIO_001121
.
}
dgn-np:NP755048.RAFbsZ27_ctYzOZU00-mzNRmfALWJfQJzWiNxpNZLuMb4130_provenance
{
dgn-np:NP755048.RAFbsZ27_ctYzOZU00-mzNRmfALWJfQJzWiNxpNZLuMb4130_assertion
dcterms:description
"[In cases of Prader-Willi syndrome (PWS), a total of 24 patients with PWS, as well as 205 control individuals from the general population, were analyzed by use of multiplex quantitative PCR to amplify the FGFR2 gene, the KRIT1 gene, and the SNRPN gene simultaneously.]. 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:17040959
;
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:NP755048.RAFbsZ27_ctYzOZU00-mzNRmfALWJfQJzWiNxpNZLuMb4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:37+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" .
}