@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP214684.RAoZ3NY8IREQAErOXHAHaSIQMqADQRueh_mf33yTnXWcw
> .
@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:NP214684.RAoZ3NY8IREQAErOXHAHaSIQMqADQRueh_mf33yTnXWcw130_head
{
this:
np:hasAssertion
dgn-np:NP214684.RAoZ3NY8IREQAErOXHAHaSIQMqADQRueh_mf33yTnXWcw130_assertion
;
np:hasProvenance
dgn-np:NP214684.RAoZ3NY8IREQAErOXHAHaSIQMqADQRueh_mf33yTnXWcw130_provenance
;
np:hasPublicationInfo
dgn-np:NP214684.RAoZ3NY8IREQAErOXHAHaSIQMqADQRueh_mf33yTnXWcw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP214684.RAoZ3NY8IREQAErOXHAHaSIQMqADQRueh_mf33yTnXWcw130_assertion
a
np:Assertion
.
dgn-np:NP214684.RAoZ3NY8IREQAErOXHAHaSIQMqADQRueh_mf33yTnXWcw130_provenance
a
np:Provenance
.
dgn-np:NP214684.RAoZ3NY8IREQAErOXHAHaSIQMqADQRueh_mf33yTnXWcw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP214684.RAoZ3NY8IREQAErOXHAHaSIQMqADQRueh_mf33yTnXWcw130_assertion
{
miriam-gene:2852
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNd92524f0faaf63fe1e5b6d309feccf4d
sio:SIO_000628
miriam-gene:2852
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP214684.RAoZ3NY8IREQAErOXHAHaSIQMqADQRueh_mf33yTnXWcw130_provenance
{
dgn-np:NP214684.RAoZ3NY8IREQAErOXHAHaSIQMqADQRueh_mf33yTnXWcw130_assertion
dcterms:description
"[Nine known SNPs and 13 artificial point mutations within the GPR30 ORF, as well as single nucleotide variants in DNA extracted from subjects with breast cancers were tested under the optimal experimental conditions.]. 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:22525040
;
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:NP214684.RAoZ3NY8IREQAErOXHAHaSIQMqADQRueh_mf33yTnXWcw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:59+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" .
}