@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP847847.RAaCEQv84KOsivnwuz3NKkZWFdlCzCdfDGw0kvyoI6d08
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP847847.RAaCEQv84KOsivnwuz3NKkZWFdlCzCdfDGw0kvyoI6d08130_head
{
this:
np:hasAssertion
dgn-np:NP847847.RAaCEQv84KOsivnwuz3NKkZWFdlCzCdfDGw0kvyoI6d08130_assertion
;
np:hasProvenance
dgn-np:NP847847.RAaCEQv84KOsivnwuz3NKkZWFdlCzCdfDGw0kvyoI6d08130_provenance
;
np:hasPublicationInfo
dgn-np:NP847847.RAaCEQv84KOsivnwuz3NKkZWFdlCzCdfDGw0kvyoI6d08130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP847847.RAaCEQv84KOsivnwuz3NKkZWFdlCzCdfDGw0kvyoI6d08130_assertion
a
np:Assertion
.
dgn-np:NP847847.RAaCEQv84KOsivnwuz3NKkZWFdlCzCdfDGw0kvyoI6d08130_provenance
a
np:Provenance
.
dgn-np:NP847847.RAaCEQv84KOsivnwuz3NKkZWFdlCzCdfDGw0kvyoI6d08130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP847847.RAaCEQv84KOsivnwuz3NKkZWFdlCzCdfDGw0kvyoI6d08130_assertion
{
miriam-gene:790
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNf1e9d9b9f37e6e419494f1acbe41cd71
sio:SIO_000628
miriam-gene:790
,
lld:C0010068
;
a
sio:SIO_001122
.
}
dgn-np:NP847847.RAaCEQv84KOsivnwuz3NKkZWFdlCzCdfDGw0kvyoI6d08130_provenance
{
dgn-np:NP847847.RAaCEQv84KOsivnwuz3NKkZWFdlCzCdfDGw0kvyoI6d08130_assertion
dcterms:description
"[A polymorphism in the corresponding FCG2RA gene resulting in an amino acid change (R131H) has been implicated, with conflicting results in the pathogenesis of various autoimmune or inflammatory disorders (e.g., atherosclerosis and coronary artery disease [CAD]).]. 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:20973705
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP847847.RAaCEQv84KOsivnwuz3NKkZWFdlCzCdfDGw0kvyoI6d08130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:09+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}