@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP217705.RAqQLX15k52NE9SvlPbDIL6BhUBmSd6S-ieQlHfyHa2Pc
> .
@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:NP217705.RAqQLX15k52NE9SvlPbDIL6BhUBmSd6S-ieQlHfyHa2Pc130_head
{
this:
np:hasAssertion
dgn-np:NP217705.RAqQLX15k52NE9SvlPbDIL6BhUBmSd6S-ieQlHfyHa2Pc130_assertion
;
np:hasProvenance
dgn-np:NP217705.RAqQLX15k52NE9SvlPbDIL6BhUBmSd6S-ieQlHfyHa2Pc130_provenance
;
np:hasPublicationInfo
dgn-np:NP217705.RAqQLX15k52NE9SvlPbDIL6BhUBmSd6S-ieQlHfyHa2Pc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP217705.RAqQLX15k52NE9SvlPbDIL6BhUBmSd6S-ieQlHfyHa2Pc130_assertion
a
np:Assertion
.
dgn-np:NP217705.RAqQLX15k52NE9SvlPbDIL6BhUBmSd6S-ieQlHfyHa2Pc130_provenance
a
np:Provenance
.
dgn-np:NP217705.RAqQLX15k52NE9SvlPbDIL6BhUBmSd6S-ieQlHfyHa2Pc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP217705.RAqQLX15k52NE9SvlPbDIL6BhUBmSd6S-ieQlHfyHa2Pc130_assertion
{
miriam-gene:7389
a
ncit:C16612
.
lld:C0032897
a
ncit:C7057
.
dgn-gda:DGNf314c07fad69b6b4a4900893ab421604
sio:SIO_000628
miriam-gene:7389
,
lld:C0032897
;
a
sio:SIO_001121
.
}
dgn-np:NP217705.RAqQLX15k52NE9SvlPbDIL6BhUBmSd6S-ieQlHfyHa2Pc130_provenance
{
dgn-np:NP217705.RAqQLX15k52NE9SvlPbDIL6BhUBmSd6S-ieQlHfyHa2Pc130_assertion
dcterms:description
"[In order to determine whether there are phenotypic differences between patients whose PWS is caused by these two different mechanisms, 54 affected individuals (37 with deletion, 17 with UPD) were personally examined and studied using molecular techniques.]. 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:9021017
;
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:NP217705.RAqQLX15k52NE9SvlPbDIL6BhUBmSd6S-ieQlHfyHa2Pc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}