@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP312140.RA6n1aKEYliHQui9urGN-lbNT06bqnE-a2a0-QWtEgT_U
> .
@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:NP312140.RA6n1aKEYliHQui9urGN-lbNT06bqnE-a2a0-QWtEgT_U130_head
{
this:
np:hasAssertion
dgn-np:NP312140.RA6n1aKEYliHQui9urGN-lbNT06bqnE-a2a0-QWtEgT_U130_assertion
;
np:hasProvenance
dgn-np:NP312140.RA6n1aKEYliHQui9urGN-lbNT06bqnE-a2a0-QWtEgT_U130_provenance
;
np:hasPublicationInfo
dgn-np:NP312140.RA6n1aKEYliHQui9urGN-lbNT06bqnE-a2a0-QWtEgT_U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP312140.RA6n1aKEYliHQui9urGN-lbNT06bqnE-a2a0-QWtEgT_U130_assertion
a
np:Assertion
.
dgn-np:NP312140.RA6n1aKEYliHQui9urGN-lbNT06bqnE-a2a0-QWtEgT_U130_provenance
a
np:Provenance
.
dgn-np:NP312140.RA6n1aKEYliHQui9urGN-lbNT06bqnE-a2a0-QWtEgT_U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP312140.RA6n1aKEYliHQui9urGN-lbNT06bqnE-a2a0-QWtEgT_U130_assertion
{
miriam-gene:51200
a
ncit:C16612
.
lld:C0175693
a
ncit:C7057
.
dgn-gda:DGN78c220039444062ae5ae5c49696c9d71
sio:SIO_000628
miriam-gene:51200
,
lld:C0175693
;
a
sio:SIO_001121
.
}
dgn-np:NP312140.RA6n1aKEYliHQui9urGN-lbNT06bqnE-a2a0-QWtEgT_U130_provenance
{
dgn-np:NP312140.RA6n1aKEYliHQui9urGN-lbNT06bqnE-a2a0-QWtEgT_U130_assertion
dcterms:description
"[As CPA4 has a potential role in cell proliferation and differentiation, two preferentially expressed copies in mUPD patients with SRS syndrome would result in excess expression and could alter the growth profiles of these subjects and give rise to intrauterine growth restriction.]. 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:12676894
;
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:NP312140.RA6n1aKEYliHQui9urGN-lbNT06bqnE-a2a0-QWtEgT_U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}