@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP603582.RACRU5Uefq9O3ft9-7DOs7ODJy9GHPJzjsVmbLHE7j334
> .
@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:NP603582.RACRU5Uefq9O3ft9-7DOs7ODJy9GHPJzjsVmbLHE7j334130_head
{
this:
np:hasAssertion
dgn-np:NP603582.RACRU5Uefq9O3ft9-7DOs7ODJy9GHPJzjsVmbLHE7j334130_assertion
;
np:hasProvenance
dgn-np:NP603582.RACRU5Uefq9O3ft9-7DOs7ODJy9GHPJzjsVmbLHE7j334130_provenance
;
np:hasPublicationInfo
dgn-np:NP603582.RACRU5Uefq9O3ft9-7DOs7ODJy9GHPJzjsVmbLHE7j334130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP603582.RACRU5Uefq9O3ft9-7DOs7ODJy9GHPJzjsVmbLHE7j334130_assertion
a
np:Assertion
.
dgn-np:NP603582.RACRU5Uefq9O3ft9-7DOs7ODJy9GHPJzjsVmbLHE7j334130_provenance
a
np:Provenance
.
dgn-np:NP603582.RACRU5Uefq9O3ft9-7DOs7ODJy9GHPJzjsVmbLHE7j334130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP603582.RACRU5Uefq9O3ft9-7DOs7ODJy9GHPJzjsVmbLHE7j334130_assertion
{
miriam-gene:2204
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN1a4d2da514adbb3161f5e1f4fe576278
sio:SIO_000628
miriam-gene:2204
,
lld:C0027051
;
a
sio:SIO_001121
.
}
dgn-np:NP603582.RACRU5Uefq9O3ft9-7DOs7ODJy9GHPJzjsVmbLHE7j334130_provenance
{
dgn-np:NP603582.RACRU5Uefq9O3ft9-7DOs7ODJy9GHPJzjsVmbLHE7j334130_assertion
dcterms:description
"[Because the myeloid IgA Fc receptor encoded by FCAR mediates inflammation, we hypothesized that the FCAR Asp92Asn polymorphism is associated with risk of MI and that this risk would be modified by pravastatin.]. 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:17008591
;
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:NP603582.RACRU5Uefq9O3ft9-7DOs7ODJy9GHPJzjsVmbLHE7j334130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:02+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" .
}