@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP576299.RAHQ2UdYwRFi7U67-u-vIAWBXV_jFg96lEvYQChS2CgrU
> .
@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:NP576299.RAHQ2UdYwRFi7U67-u-vIAWBXV_jFg96lEvYQChS2CgrU130_head
{
this:
np:hasAssertion
dgn-np:NP576299.RAHQ2UdYwRFi7U67-u-vIAWBXV_jFg96lEvYQChS2CgrU130_assertion
;
np:hasProvenance
dgn-np:NP576299.RAHQ2UdYwRFi7U67-u-vIAWBXV_jFg96lEvYQChS2CgrU130_provenance
;
np:hasPublicationInfo
dgn-np:NP576299.RAHQ2UdYwRFi7U67-u-vIAWBXV_jFg96lEvYQChS2CgrU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP576299.RAHQ2UdYwRFi7U67-u-vIAWBXV_jFg96lEvYQChS2CgrU130_assertion
a
np:Assertion
.
dgn-np:NP576299.RAHQ2UdYwRFi7U67-u-vIAWBXV_jFg96lEvYQChS2CgrU130_provenance
a
np:Provenance
.
dgn-np:NP576299.RAHQ2UdYwRFi7U67-u-vIAWBXV_jFg96lEvYQChS2CgrU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP576299.RAHQ2UdYwRFi7U67-u-vIAWBXV_jFg96lEvYQChS2CgrU130_assertion
{
miriam-gene:185
a
ncit:C16612
.
lld:C0000786
a
ncit:C7057
.
dgn-gda:DGN75b4fc497654c0c565df42d05e8f2453
sio:SIO_000628
miriam-gene:185
,
lld:C0000786
;
a
sio:SIO_001121
.
}
dgn-np:NP576299.RAHQ2UdYwRFi7U67-u-vIAWBXV_jFg96lEvYQChS2CgrU130_provenance
{
dgn-np:NP576299.RAHQ2UdYwRFi7U67-u-vIAWBXV_jFg96lEvYQChS2CgrU130_assertion
dcterms:description
"[The aim of our study was to investigate, whether two polymorphisms in the AT1R and NOS3 genes shown to result in maternal vasoconstriction are associated with an increased risk for RSA.]. 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:15212666
;
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:NP576299.RAHQ2UdYwRFi7U67-u-vIAWBXV_jFg96lEvYQChS2CgrU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:47+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" .
}