@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP331031.RA0557Na-Rz9t5azAjeK_q_d5xmAacx60EqY6hACWkp9Q
> .
@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:NP331031.RA0557Na-Rz9t5azAjeK_q_d5xmAacx60EqY6hACWkp9Q130_head
{
this:
np:hasAssertion
dgn-np:NP331031.RA0557Na-Rz9t5azAjeK_q_d5xmAacx60EqY6hACWkp9Q130_assertion
;
np:hasProvenance
dgn-np:NP331031.RA0557Na-Rz9t5azAjeK_q_d5xmAacx60EqY6hACWkp9Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP331031.RA0557Na-Rz9t5azAjeK_q_d5xmAacx60EqY6hACWkp9Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP331031.RA0557Na-Rz9t5azAjeK_q_d5xmAacx60EqY6hACWkp9Q130_assertion
a
np:Assertion
.
dgn-np:NP331031.RA0557Na-Rz9t5azAjeK_q_d5xmAacx60EqY6hACWkp9Q130_provenance
a
np:Provenance
.
dgn-np:NP331031.RA0557Na-Rz9t5azAjeK_q_d5xmAacx60EqY6hACWkp9Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP331031.RA0557Na-Rz9t5azAjeK_q_d5xmAacx60EqY6hACWkp9Q130_assertion
{
miriam-gene:7389
a
ncit:C16612
.
lld:C0036572
a
ncit:C7057
.
dgn-gda:DGN5495171b187d18c925d9208e700789fc
sio:SIO_000628
miriam-gene:7389
,
lld:C0036572
;
a
sio:SIO_001121
.
}
dgn-np:NP331031.RA0557Na-Rz9t5azAjeK_q_d5xmAacx60EqY6hACWkp9Q130_provenance
{
dgn-np:NP331031.RA0557Na-Rz9t5azAjeK_q_d5xmAacx60EqY6hACWkp9Q130_assertion
dcterms:description
"[Comparing the clinical pictures of our patients with UPD with those with deletions, we found that UPD children presented with lower birth length and started walking earlier and deletion patients presented with a much higher incidence of seizures than UPD patients.]. 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:15617548
;
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:NP331031.RA0557Na-Rz9t5azAjeK_q_d5xmAacx60EqY6hACWkp9Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:15+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" .
}