@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP840756.RAjjEFN-NaFxLoamTCw-M06lQxgLIcGmtyLPcdNPilPds
> .
@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:NP840756.RAjjEFN-NaFxLoamTCw-M06lQxgLIcGmtyLPcdNPilPds130_head
{
this:
np:hasAssertion
dgn-np:NP840756.RAjjEFN-NaFxLoamTCw-M06lQxgLIcGmtyLPcdNPilPds130_assertion
;
np:hasProvenance
dgn-np:NP840756.RAjjEFN-NaFxLoamTCw-M06lQxgLIcGmtyLPcdNPilPds130_provenance
;
np:hasPublicationInfo
dgn-np:NP840756.RAjjEFN-NaFxLoamTCw-M06lQxgLIcGmtyLPcdNPilPds130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP840756.RAjjEFN-NaFxLoamTCw-M06lQxgLIcGmtyLPcdNPilPds130_assertion
a
np:Assertion
.
dgn-np:NP840756.RAjjEFN-NaFxLoamTCw-M06lQxgLIcGmtyLPcdNPilPds130_provenance
a
np:Provenance
.
dgn-np:NP840756.RAjjEFN-NaFxLoamTCw-M06lQxgLIcGmtyLPcdNPilPds130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP840756.RAjjEFN-NaFxLoamTCw-M06lQxgLIcGmtyLPcdNPilPds130_assertion
{
miriam-gene:11117
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGNd150330e730bef7b6ca93c4fffa0285c
sio:SIO_000628
miriam-gene:11117
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP840756.RAjjEFN-NaFxLoamTCw-M06lQxgLIcGmtyLPcdNPilPds130_provenance
{
dgn-np:NP840756.RAjjEFN-NaFxLoamTCw-M06lQxgLIcGmtyLPcdNPilPds130_assertion
dcterms:description
"[We confirmed that rs2289360, rs2011616, and rs2304682 in the human EMILIN1 gene, as well as the haplotype constructed using rs2536512, rs2011616, and rs17881426 are useful genetic markers of EH in Japanese men.]. 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:20186130
;
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:NP840756.RAjjEFN-NaFxLoamTCw-M06lQxgLIcGmtyLPcdNPilPds130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:34+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" .
}