@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP692036.RATiPCIeG6OTX-rj2Gx-hW5F9mSSk3wI2p0yKTviv33RQ
> .
@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:NP692036.RATiPCIeG6OTX-rj2Gx-hW5F9mSSk3wI2p0yKTviv33RQ130_head
{
this:
np:hasAssertion
dgn-np:NP692036.RATiPCIeG6OTX-rj2Gx-hW5F9mSSk3wI2p0yKTviv33RQ130_assertion
;
np:hasProvenance
dgn-np:NP692036.RATiPCIeG6OTX-rj2Gx-hW5F9mSSk3wI2p0yKTviv33RQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP692036.RATiPCIeG6OTX-rj2Gx-hW5F9mSSk3wI2p0yKTviv33RQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP692036.RATiPCIeG6OTX-rj2Gx-hW5F9mSSk3wI2p0yKTviv33RQ130_assertion
a
np:Assertion
.
dgn-np:NP692036.RATiPCIeG6OTX-rj2Gx-hW5F9mSSk3wI2p0yKTviv33RQ130_provenance
a
np:Provenance
.
dgn-np:NP692036.RATiPCIeG6OTX-rj2Gx-hW5F9mSSk3wI2p0yKTviv33RQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP692036.RATiPCIeG6OTX-rj2Gx-hW5F9mSSk3wI2p0yKTviv33RQ130_assertion
{
miriam-gene:267012
a
ncit:C16612
.
lld:C1852197
a
ncit:C7057
.
dgn-gda:DGNa549d0abf4adda5a2b5c227069c882ee
sio:SIO_000628
miriam-gene:267012
,
lld:C1852197
;
a
sio:SIO_001121
.
}
dgn-np:NP692036.RATiPCIeG6OTX-rj2Gx-hW5F9mSSk3wI2p0yKTviv33RQ130_provenance
{
dgn-np:NP692036.RATiPCIeG6OTX-rj2Gx-hW5F9mSSk3wI2p0yKTviv33RQ130_assertion
dcterms:description
"[Although the associated alleles and haplotypes differ from those previously reported, these new results provide further evidence, in an independent sample, for an association between BPAD and genetic variation in the vicinity of the genes G72 and G30.]. 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:14699445
;
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:NP692036.RATiPCIeG6OTX-rj2Gx-hW5F9mSSk3wI2p0yKTviv33RQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:00+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" .
}