@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP256999.RAB4CwdQJc-Qgusjb030vFAGMvuMLValGxkymrq0bnRgY
> .
@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:NP256999.RAB4CwdQJc-Qgusjb030vFAGMvuMLValGxkymrq0bnRgY130_head
{
this:
np:hasAssertion
dgn-np:NP256999.RAB4CwdQJc-Qgusjb030vFAGMvuMLValGxkymrq0bnRgY130_assertion
;
np:hasProvenance
dgn-np:NP256999.RAB4CwdQJc-Qgusjb030vFAGMvuMLValGxkymrq0bnRgY130_provenance
;
np:hasPublicationInfo
dgn-np:NP256999.RAB4CwdQJc-Qgusjb030vFAGMvuMLValGxkymrq0bnRgY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP256999.RAB4CwdQJc-Qgusjb030vFAGMvuMLValGxkymrq0bnRgY130_assertion
a
np:Assertion
.
dgn-np:NP256999.RAB4CwdQJc-Qgusjb030vFAGMvuMLValGxkymrq0bnRgY130_provenance
a
np:Provenance
.
dgn-np:NP256999.RAB4CwdQJc-Qgusjb030vFAGMvuMLValGxkymrq0bnRgY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP256999.RAB4CwdQJc-Qgusjb030vFAGMvuMLValGxkymrq0bnRgY130_assertion
{
miriam-gene:5003
a
ncit:C16612
.
lld:C0004903
a
ncit:C7057
.
dgn-gda:DGNdb0827b4a4d5c246499ee6145ebb0528
sio:SIO_000628
miriam-gene:5003
,
lld:C0004903
;
a
sio:SIO_001121
.
}
dgn-np:NP256999.RAB4CwdQJc-Qgusjb030vFAGMvuMLValGxkymrq0bnRgY130_provenance
{
dgn-np:NP256999.RAB4CwdQJc-Qgusjb030vFAGMvuMLValGxkymrq0bnRgY130_assertion
dcterms:description
"[Although SSCP analysis of 62 WT samples and 10 BWS patients did not result in the identification of any mutations in ORCTL2 or ORCTL2S, it will be important to examine their expression pattern in tumors and BWS patients, since epigenetic alteration at these loci may play a role in the etiology of these diseases.]. 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:9570947
;
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:NP256999.RAB4CwdQJc-Qgusjb030vFAGMvuMLValGxkymrq0bnRgY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:23+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" .
}