@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP677599.RAddnpkx-MBP9aeQ3S-pZXOegWBl31XWz4WRdwEdkp6Xk
> .
@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:NP677599.RAddnpkx-MBP9aeQ3S-pZXOegWBl31XWz4WRdwEdkp6Xk130_head
{
this:
np:hasAssertion
dgn-np:NP677599.RAddnpkx-MBP9aeQ3S-pZXOegWBl31XWz4WRdwEdkp6Xk130_assertion
;
np:hasProvenance
dgn-np:NP677599.RAddnpkx-MBP9aeQ3S-pZXOegWBl31XWz4WRdwEdkp6Xk130_provenance
;
np:hasPublicationInfo
dgn-np:NP677599.RAddnpkx-MBP9aeQ3S-pZXOegWBl31XWz4WRdwEdkp6Xk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP677599.RAddnpkx-MBP9aeQ3S-pZXOegWBl31XWz4WRdwEdkp6Xk130_assertion
a
np:Assertion
.
dgn-np:NP677599.RAddnpkx-MBP9aeQ3S-pZXOegWBl31XWz4WRdwEdkp6Xk130_provenance
a
np:Provenance
.
dgn-np:NP677599.RAddnpkx-MBP9aeQ3S-pZXOegWBl31XWz4WRdwEdkp6Xk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP677599.RAddnpkx-MBP9aeQ3S-pZXOegWBl31XWz4WRdwEdkp6Xk130_assertion
{
miriam-gene:10019
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN43a9faf9858bcdb0e7d43bd826e795ae
sio:SIO_000628
miriam-gene:10019
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP677599.RAddnpkx-MBP9aeQ3S-pZXOegWBl31XWz4WRdwEdkp6Xk130_provenance
{
dgn-np:NP677599.RAddnpkx-MBP9aeQ3S-pZXOegWBl31XWz4WRdwEdkp6Xk130_assertion
dcterms:description
"[Overall, although we confirmed one locus (SH2B3) as associated with both kidney and cardiovascular disease, our primary findings suggest that there is little overlap between kidney and cardiovascular disease risk variants in the overall population.]. 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:23474010
;
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:NP677599.RAddnpkx-MBP9aeQ3S-pZXOegWBl31XWz4WRdwEdkp6Xk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:49+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" .
}