@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs
> .
@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:NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_head
{
this:
np:hasAssertion
dgn-np:NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_assertion
;
np:hasProvenance
dgn-np:NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_provenance
;
np:hasPublicationInfo
dgn-np:NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_assertion
a
np:Assertion
.
dgn-np:NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_provenance
a
np:Provenance
.
dgn-np:NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_assertion
{
miriam-gene:6047
a
ncit:C16612
.
lld:C0032897
a
ncit:C7057
.
dgn-gda:DGNa87119912947a47d2a42c3239e7fa9eb
sio:SIO_000628
miriam-gene:6047
,
lld:C0032897
;
a
sio:SIO_001121
.
}
dgn-np:NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_provenance
{
dgn-np:NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_assertion
dcterms:description
"[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. 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:17262171
;
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:NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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" .
}