@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP552473.RAw2BFokk0DKpU0tgEu3vMnAdsvUT6h8hEppYavMHwQdk
> .
@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:NP552473.RAw2BFokk0DKpU0tgEu3vMnAdsvUT6h8hEppYavMHwQdk130_head
{
this:
np:hasAssertion
dgn-np:NP552473.RAw2BFokk0DKpU0tgEu3vMnAdsvUT6h8hEppYavMHwQdk130_assertion
;
np:hasProvenance
dgn-np:NP552473.RAw2BFokk0DKpU0tgEu3vMnAdsvUT6h8hEppYavMHwQdk130_provenance
;
np:hasPublicationInfo
dgn-np:NP552473.RAw2BFokk0DKpU0tgEu3vMnAdsvUT6h8hEppYavMHwQdk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP552473.RAw2BFokk0DKpU0tgEu3vMnAdsvUT6h8hEppYavMHwQdk130_assertion
a
np:Assertion
.
dgn-np:NP552473.RAw2BFokk0DKpU0tgEu3vMnAdsvUT6h8hEppYavMHwQdk130_provenance
a
np:Provenance
.
dgn-np:NP552473.RAw2BFokk0DKpU0tgEu3vMnAdsvUT6h8hEppYavMHwQdk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP552473.RAw2BFokk0DKpU0tgEu3vMnAdsvUT6h8hEppYavMHwQdk130_assertion
{
miriam-gene:4948
a
ncit:C16612
.
lld:C0032897
a
ncit:C7057
.
dgn-gda:DGNc549f06671080ff081b197542b71a3a8
sio:SIO_000628
miriam-gene:4948
,
lld:C0032897
;
a
sio:SIO_001121
.
}
dgn-np:NP552473.RAw2BFokk0DKpU0tgEu3vMnAdsvUT6h8hEppYavMHwQdk130_provenance
{
dgn-np:NP552473.RAw2BFokk0DKpU0tgEu3vMnAdsvUT6h8hEppYavMHwQdk130_assertion
dcterms:description
"[Cases of PWS due to UPD do not appear to differ from those due to deletion (hypopigmentation in deletional cases can be explained by loss of D15S12 downstream from the critical region).]. 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:8872029
;
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:NP552473.RAw2BFokk0DKpU0tgEu3vMnAdsvUT6h8hEppYavMHwQdk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:33+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" .
}