@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP200712.RApbbnGFbtQp15vd5rREOi5dB7CBtkG7rJnmpJcIVHKvQ
> .
@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:NP200712.RApbbnGFbtQp15vd5rREOi5dB7CBtkG7rJnmpJcIVHKvQ130_head
{
this:
np:hasAssertion
dgn-np:NP200712.RApbbnGFbtQp15vd5rREOi5dB7CBtkG7rJnmpJcIVHKvQ130_assertion
;
np:hasProvenance
dgn-np:NP200712.RApbbnGFbtQp15vd5rREOi5dB7CBtkG7rJnmpJcIVHKvQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP200712.RApbbnGFbtQp15vd5rREOi5dB7CBtkG7rJnmpJcIVHKvQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP200712.RApbbnGFbtQp15vd5rREOi5dB7CBtkG7rJnmpJcIVHKvQ130_assertion
a
np:Assertion
.
dgn-np:NP200712.RApbbnGFbtQp15vd5rREOi5dB7CBtkG7rJnmpJcIVHKvQ130_provenance
a
np:Provenance
.
dgn-np:NP200712.RApbbnGFbtQp15vd5rREOi5dB7CBtkG7rJnmpJcIVHKvQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP200712.RApbbnGFbtQp15vd5rREOi5dB7CBtkG7rJnmpJcIVHKvQ130_assertion
{
miriam-gene:2247
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGNbe0e83a82ec283fc7898f0fc9f12c9d8
sio:SIO_000628
miriam-gene:2247
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP200712.RApbbnGFbtQp15vd5rREOi5dB7CBtkG7rJnmpJcIVHKvQ130_provenance
{
dgn-np:NP200712.RApbbnGFbtQp15vd5rREOi5dB7CBtkG7rJnmpJcIVHKvQ130_assertion
dcterms:description
"[The impact of bFGF gene polymorphisms on serum bFGF levels was also investigated and significantly higher serum levels of bFGF were demonstrated in diabetes patients with the TA genotype of the -553 T/A polymorphism compared with diabetes patients with the TT wild type genotype (9.0 +/- 5.6 ng/l versus 3.0 +/- 1.9 ng/l, respectively).]. 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:19930868
;
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:NP200712.RApbbnGFbtQp15vd5rREOi5dB7CBtkG7rJnmpJcIVHKvQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:50+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" .
}