@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP145766.RAUPNnhQtbPJzVIvQSHQ3LzziollJqLGigCTrImgMr8Eo
> .
@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:NP145766.RAUPNnhQtbPJzVIvQSHQ3LzziollJqLGigCTrImgMr8Eo130_head
{
this:
np:hasAssertion
dgn-np:NP145766.RAUPNnhQtbPJzVIvQSHQ3LzziollJqLGigCTrImgMr8Eo130_assertion
;
np:hasProvenance
dgn-np:NP145766.RAUPNnhQtbPJzVIvQSHQ3LzziollJqLGigCTrImgMr8Eo130_provenance
;
np:hasPublicationInfo
dgn-np:NP145766.RAUPNnhQtbPJzVIvQSHQ3LzziollJqLGigCTrImgMr8Eo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP145766.RAUPNnhQtbPJzVIvQSHQ3LzziollJqLGigCTrImgMr8Eo130_assertion
a
np:Assertion
.
dgn-np:NP145766.RAUPNnhQtbPJzVIvQSHQ3LzziollJqLGigCTrImgMr8Eo130_provenance
a
np:Provenance
.
dgn-np:NP145766.RAUPNnhQtbPJzVIvQSHQ3LzziollJqLGigCTrImgMr8Eo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP145766.RAUPNnhQtbPJzVIvQSHQ3LzziollJqLGigCTrImgMr8Eo130_assertion
{
miriam-gene:1026
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGN961c5a61216693e131a7f8dd43b8362a
sio:SIO_000628
miriam-gene:1026
,
lld:C0007137
;
a
sio:SIO_001122
.
}
dgn-np:NP145766.RAUPNnhQtbPJzVIvQSHQ3LzziollJqLGigCTrImgMr8Eo130_provenance
{
dgn-np:NP145766.RAUPNnhQtbPJzVIvQSHQ3LzziollJqLGigCTrImgMr8Eo130_assertion
dcterms:description
"[Our findings indicated that codon 31 Ser allele homozygosity, either alone or in combination with the other two SNPs, may be associated with development of EC. These findings warrant validation in a larger study of EC patients.]. 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:20112071
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP145766.RAUPNnhQtbPJzVIvQSHQ3LzziollJqLGigCTrImgMr8Eo130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:01+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" .
}