@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1333018.RAofEI4CcYoOZLTsagD5k_QWsq_e9Rsa4Wrx5VIYJ0e1w
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1333018.RAofEI4CcYoOZLTsagD5k_QWsq_e9Rsa4Wrx5VIYJ0e1w130_head
{
this:
np:hasAssertion
dgn-np:NP1333018.RAofEI4CcYoOZLTsagD5k_QWsq_e9Rsa4Wrx5VIYJ0e1w130_assertion
;
np:hasProvenance
dgn-np:NP1333018.RAofEI4CcYoOZLTsagD5k_QWsq_e9Rsa4Wrx5VIYJ0e1w130_provenance
;
np:hasPublicationInfo
dgn-np:NP1333018.RAofEI4CcYoOZLTsagD5k_QWsq_e9Rsa4Wrx5VIYJ0e1w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1333018.RAofEI4CcYoOZLTsagD5k_QWsq_e9Rsa4Wrx5VIYJ0e1w130_assertion
a
np:Assertion
.
dgn-np:NP1333018.RAofEI4CcYoOZLTsagD5k_QWsq_e9Rsa4Wrx5VIYJ0e1w130_provenance
a
np:Provenance
.
dgn-np:NP1333018.RAofEI4CcYoOZLTsagD5k_QWsq_e9Rsa4Wrx5VIYJ0e1w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1333018.RAofEI4CcYoOZLTsagD5k_QWsq_e9Rsa4Wrx5VIYJ0e1w130_assertion
{
miriam-gene:6638
a
ncit:C16612
.
lld:C0032897
a
ncit:C7057
.
dgn-gda:DGNa77b6be1e4190c9d1fd993a733b8aa7c
sio:SIO_000628
miriam-gene:6638
,
lld:C0032897
;
a
sio:SIO_001121
.
}
dgn-np:NP1333018.RAofEI4CcYoOZLTsagD5k_QWsq_e9Rsa4Wrx5VIYJ0e1w130_provenance
{
dgn-np:NP1333018.RAofEI4CcYoOZLTsagD5k_QWsq_e9Rsa4Wrx5VIYJ0e1w130_assertion
dcterms:description
"[Our findings indicate that SNRPN is expressed only from the paternally derived chromosome 15 in humans and therefore may fulfill one major criterion for being involved in the pathogenesis of the Prader-Willi 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:8111367
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1333018.RAofEI4CcYoOZLTsagD5k_QWsq_e9Rsa4Wrx5VIYJ0e1w130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:50+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}