@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_head
{
this:
np:hasAssertion
dgn-np:NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_assertion
;
np:hasProvenance
dgn-np:NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_provenance
;
np:hasPublicationInfo
dgn-np:NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_assertion
a
np:Assertion
.
dgn-np:NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_provenance
a
np:Provenance
.
dgn-np:NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_assertion
{
miriam-gene:25942
a
ncit:C16612
.
lld:C3697269
a
ncit:C7057
.
dgn-gda:DGNbc3699bfba14d98e2ef4b0ffe81f044f
sio:SIO_000628
miriam-gene:25942
,
lld:C3697269
;
a
sio:SIO_001121
.
}
dgn-np:NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_provenance
{
dgn-np:NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_assertion
dcterms:description
"[There are several candidate genes within the SRO, including CYP11A1, SEMA7A, CPLX3, ARID3B, STRA6, SIN3A and CSK, that may predispose to many of the clinical features observed in individuals with 15q24 deletion syndrome.]. 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:22216833
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:36+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}