@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP868069.RAPefv7n5AO-_BhjDU84GNUq92uFh5XD2Ybd55PjXKn8I
> .
@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:NP868069.RAPefv7n5AO-_BhjDU84GNUq92uFh5XD2Ybd55PjXKn8I130_head
{
this:
np:hasAssertion
dgn-np:NP868069.RAPefv7n5AO-_BhjDU84GNUq92uFh5XD2Ybd55PjXKn8I130_assertion
;
np:hasProvenance
dgn-np:NP868069.RAPefv7n5AO-_BhjDU84GNUq92uFh5XD2Ybd55PjXKn8I130_provenance
;
np:hasPublicationInfo
dgn-np:NP868069.RAPefv7n5AO-_BhjDU84GNUq92uFh5XD2Ybd55PjXKn8I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP868069.RAPefv7n5AO-_BhjDU84GNUq92uFh5XD2Ybd55PjXKn8I130_assertion
a
np:Assertion
.
dgn-np:NP868069.RAPefv7n5AO-_BhjDU84GNUq92uFh5XD2Ybd55PjXKn8I130_provenance
a
np:Provenance
.
dgn-np:NP868069.RAPefv7n5AO-_BhjDU84GNUq92uFh5XD2Ybd55PjXKn8I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP868069.RAPefv7n5AO-_BhjDU84GNUq92uFh5XD2Ybd55PjXKn8I130_assertion
{
miriam-gene:8856
a
ncit:C16612
.
lld:C0032897
a
ncit:C7057
.
dgn-gda:DGN7f1b93606a59b993dde5d77ed473f751
sio:SIO_000628
miriam-gene:8856
,
lld:C0032897
;
a
sio:SIO_001121
.
}
dgn-np:NP868069.RAPefv7n5AO-_BhjDU84GNUq92uFh5XD2Ybd55PjXKn8I130_provenance
{
dgn-np:NP868069.RAPefv7n5AO-_BhjDU84GNUq92uFh5XD2Ybd55PjXKn8I130_assertion
dcterms:description
"[Within 15q11-q13, four genes (SNRPN, IPW, ZNF127, FNZ127) and two expressed sequence tags (PAR1 and PAR5) have been found to be expressed only from the paternally inherited chromosome, and therefore all must be considered candidate genes involved in the pathogenesis of PWS.]. 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:9237260
;
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:NP868069.RAPefv7n5AO-_BhjDU84GNUq92uFh5XD2Ybd55PjXKn8I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:50+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" .
}