@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP141523.RAPvkL-5yPoI2g9yZqaormdcic8waVtkpsfMM7NWBJMKE
> .
@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:NP141523.RAPvkL-5yPoI2g9yZqaormdcic8waVtkpsfMM7NWBJMKE130_head
{
this:
np:hasAssertion
dgn-np:NP141523.RAPvkL-5yPoI2g9yZqaormdcic8waVtkpsfMM7NWBJMKE130_assertion
;
np:hasProvenance
dgn-np:NP141523.RAPvkL-5yPoI2g9yZqaormdcic8waVtkpsfMM7NWBJMKE130_provenance
;
np:hasPublicationInfo
dgn-np:NP141523.RAPvkL-5yPoI2g9yZqaormdcic8waVtkpsfMM7NWBJMKE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP141523.RAPvkL-5yPoI2g9yZqaormdcic8waVtkpsfMM7NWBJMKE130_assertion
a
np:Assertion
.
dgn-np:NP141523.RAPvkL-5yPoI2g9yZqaormdcic8waVtkpsfMM7NWBJMKE130_provenance
a
np:Provenance
.
dgn-np:NP141523.RAPvkL-5yPoI2g9yZqaormdcic8waVtkpsfMM7NWBJMKE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP141523.RAPvkL-5yPoI2g9yZqaormdcic8waVtkpsfMM7NWBJMKE130_assertion
{
miriam-gene:2157
a
ncit:C16612
.
lld:C0042487
a
ncit:C7057
.
dgn-gda:DGN26e4ea9d6d9a7ec6ea78473d0f65d458
sio:SIO_000628
miriam-gene:2157
,
lld:C0042487
;
a
sio:SIO_001123
.
}
dgn-np:NP141523.RAPvkL-5yPoI2g9yZqaormdcic8waVtkpsfMM7NWBJMKE130_provenance
{
dgn-np:NP141523.RAPvkL-5yPoI2g9yZqaormdcic8waVtkpsfMM7NWBJMKE130_assertion
dcterms:description
"[there are associations between several AQP2 SNPs and the risk of venous thrombosis, and weak associations with arterial blood pressure, but not with plasma levels of VWF propeptide, VWF or FVIII ]. 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:18515885
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP141523.RAPvkL-5yPoI2g9yZqaormdcic8waVtkpsfMM7NWBJMKE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:14+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" .
}