@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP562574.RAMxqEh5t4kz-FAl12p3NczW9HjEU5GjfqVXaxiVv4SOw
> .
@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:NP562574.RAMxqEh5t4kz-FAl12p3NczW9HjEU5GjfqVXaxiVv4SOw130_head
{
this:
np:hasAssertion
dgn-np:NP562574.RAMxqEh5t4kz-FAl12p3NczW9HjEU5GjfqVXaxiVv4SOw130_assertion
;
np:hasProvenance
dgn-np:NP562574.RAMxqEh5t4kz-FAl12p3NczW9HjEU5GjfqVXaxiVv4SOw130_provenance
;
np:hasPublicationInfo
dgn-np:NP562574.RAMxqEh5t4kz-FAl12p3NczW9HjEU5GjfqVXaxiVv4SOw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP562574.RAMxqEh5t4kz-FAl12p3NczW9HjEU5GjfqVXaxiVv4SOw130_assertion
a
np:Assertion
.
dgn-np:NP562574.RAMxqEh5t4kz-FAl12p3NczW9HjEU5GjfqVXaxiVv4SOw130_provenance
a
np:Provenance
.
dgn-np:NP562574.RAMxqEh5t4kz-FAl12p3NczW9HjEU5GjfqVXaxiVv4SOw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP562574.RAMxqEh5t4kz-FAl12p3NczW9HjEU5GjfqVXaxiVv4SOw130_assertion
{
miriam-gene:1401
a
ncit:C16612
.
lld:C0017921
a
ncit:C7057
.
dgn-gda:DGN091b364651ba06bc543f722310f8c07d
sio:SIO_000628
miriam-gene:1401
,
lld:C0017921
;
a
sio:SIO_001121
.
}
dgn-np:NP562574.RAMxqEh5t4kz-FAl12p3NczW9HjEU5GjfqVXaxiVv4SOw130_provenance
{
dgn-np:NP562574.RAMxqEh5t4kz-FAl12p3NczW9HjEU5GjfqVXaxiVv4SOw130_assertion
dcterms:description
"[We provide evidence that if elevated serum/plasma levels of CRP are associated with neovascular AMD, it is likely not due to genetic variation within CRP, but likely due to variations in some other genetic as well as epidemiological factors.]. 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:18704199
;
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:NP562574.RAMxqEh5t4kz-FAl12p3NczW9HjEU5GjfqVXaxiVv4SOw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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" .
}