@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP803271.RADl1W57nIMbr6NIGnvSi5wROj4ddqGqaw8hztgtGiqac
> .
@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:NP803271.RADl1W57nIMbr6NIGnvSi5wROj4ddqGqaw8hztgtGiqac130_head
{
this:
np:hasAssertion
dgn-np:NP803271.RADl1W57nIMbr6NIGnvSi5wROj4ddqGqaw8hztgtGiqac130_assertion
;
np:hasProvenance
dgn-np:NP803271.RADl1W57nIMbr6NIGnvSi5wROj4ddqGqaw8hztgtGiqac130_provenance
;
np:hasPublicationInfo
dgn-np:NP803271.RADl1W57nIMbr6NIGnvSi5wROj4ddqGqaw8hztgtGiqac130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP803271.RADl1W57nIMbr6NIGnvSi5wROj4ddqGqaw8hztgtGiqac130_assertion
a
np:Assertion
.
dgn-np:NP803271.RADl1W57nIMbr6NIGnvSi5wROj4ddqGqaw8hztgtGiqac130_provenance
a
np:Provenance
.
dgn-np:NP803271.RADl1W57nIMbr6NIGnvSi5wROj4ddqGqaw8hztgtGiqac130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP803271.RADl1W57nIMbr6NIGnvSi5wROj4ddqGqaw8hztgtGiqac130_assertion
{
miriam-gene:133
a
ncit:C16612
.
lld:C0036690
a
ncit:C7057
.
dgn-gda:DGNfdcd4585d6e2cfd89b4335e7602093d4
sio:SIO_000628
miriam-gene:133
,
lld:C0036690
;
a
sio:SIO_001121
.
}
dgn-np:NP803271.RADl1W57nIMbr6NIGnvSi5wROj4ddqGqaw8hztgtGiqac130_provenance
{
dgn-np:NP803271.RADl1W57nIMbr6NIGnvSi5wROj4ddqGqaw8hztgtGiqac130_assertion
dcterms:description
"[Specifically, we find that certain conditions, such as pregnancy, cardiovascular disease, and sepsis, are associated with robust and dynamic changes in the expression of AM and AM receptor proteins, which together represent an elegant mechanism for altering the physiological responsiveness or function of AM.]. 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:17053041
;
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:NP803271.RADl1W57nIMbr6NIGnvSi5wROj4ddqGqaw8hztgtGiqac130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:12+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" .
}