@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4
> .
@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:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_head
{
this:
np:hasAssertion
dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_assertion
;
np:hasProvenance
dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_provenance
;
np:hasPublicationInfo
dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_assertion
a
np:Assertion
.
dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_provenance
a
np:Provenance
.
dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_assertion
{
miriam-gene:7389
a
ncit:C16612
.
lld:C0162835
a
ncit:C7057
.
dgn-gda:DGNa6283c23141b95e3c10c70f9420f01de
sio:SIO_000628
miriam-gene:7389
,
lld:C0162835
;
a
sio:SIO_001121
.
}
dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_provenance
{
dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_assertion
dcterms:description
"[In addition to a higher frequency of hypopigmentation among deletion patients, minor phenotypic differences between deletion and UPD patients have recently been reported, including lower birth weight in the deletion group, shorter birth length in males with UPD, and shorter course of gavage feeding and later onset of hyperphagia in females with UPD.]. 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:9215778
;
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:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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" .
}