@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP872319.RAYPkHh0LjPinEAM1qxLk6QmD-Zh7BJHG_MxsuaDiYdMI
> .
@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:NP872319.RAYPkHh0LjPinEAM1qxLk6QmD-Zh7BJHG_MxsuaDiYdMI130_head
{
this:
np:hasAssertion
dgn-np:NP872319.RAYPkHh0LjPinEAM1qxLk6QmD-Zh7BJHG_MxsuaDiYdMI130_assertion
;
np:hasProvenance
dgn-np:NP872319.RAYPkHh0LjPinEAM1qxLk6QmD-Zh7BJHG_MxsuaDiYdMI130_provenance
;
np:hasPublicationInfo
dgn-np:NP872319.RAYPkHh0LjPinEAM1qxLk6QmD-Zh7BJHG_MxsuaDiYdMI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP872319.RAYPkHh0LjPinEAM1qxLk6QmD-Zh7BJHG_MxsuaDiYdMI130_assertion
a
np:Assertion
.
dgn-np:NP872319.RAYPkHh0LjPinEAM1qxLk6QmD-Zh7BJHG_MxsuaDiYdMI130_provenance
a
np:Provenance
.
dgn-np:NP872319.RAYPkHh0LjPinEAM1qxLk6QmD-Zh7BJHG_MxsuaDiYdMI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP872319.RAYPkHh0LjPinEAM1qxLk6QmD-Zh7BJHG_MxsuaDiYdMI130_assertion
{
miriam-gene:4855
a
ncit:C16612
.
lld:C0005586
a
ncit:C7057
.
dgn-gda:DGN21e575f24f4624fb5ff456aab8ef98bb
sio:SIO_000628
miriam-gene:4855
,
lld:C0005586
;
a
sio:SIO_001121
.
}
dgn-np:NP872319.RAYPkHh0LjPinEAM1qxLk6QmD-Zh7BJHG_MxsuaDiYdMI130_provenance
{
dgn-np:NP872319.RAYPkHh0LjPinEAM1qxLk6QmD-Zh7BJHG_MxsuaDiYdMI130_assertion
dcterms:description
"[A major consortium study have recently linked BD to hundreds of variations with stronger associations in the MHC region, such as the rs3130297 SNP, located in the NOTCH4 gene, with an additional overlapping association with schizophrenia.]. 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:21987052
;
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:NP872319.RAYPkHh0LjPinEAM1qxLk6QmD-Zh7BJHG_MxsuaDiYdMI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:53+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" .
}