@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44065.RATjQbmcE9pxUDRspkXnlCUN_GCyWNsBvyhmvGvi-Hqvk
> .
@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:NP44065.RATjQbmcE9pxUDRspkXnlCUN_GCyWNsBvyhmvGvi-Hqvk130_head
{
this:
np:hasAssertion
dgn-np:NP44065.RATjQbmcE9pxUDRspkXnlCUN_GCyWNsBvyhmvGvi-Hqvk130_assertion
;
np:hasProvenance
dgn-np:NP44065.RATjQbmcE9pxUDRspkXnlCUN_GCyWNsBvyhmvGvi-Hqvk130_provenance
;
np:hasPublicationInfo
dgn-np:NP44065.RATjQbmcE9pxUDRspkXnlCUN_GCyWNsBvyhmvGvi-Hqvk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44065.RATjQbmcE9pxUDRspkXnlCUN_GCyWNsBvyhmvGvi-Hqvk130_assertion
a
np:Assertion
.
dgn-np:NP44065.RATjQbmcE9pxUDRspkXnlCUN_GCyWNsBvyhmvGvi-Hqvk130_provenance
a
np:Provenance
.
dgn-np:NP44065.RATjQbmcE9pxUDRspkXnlCUN_GCyWNsBvyhmvGvi-Hqvk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44065.RATjQbmcE9pxUDRspkXnlCUN_GCyWNsBvyhmvGvi-Hqvk130_assertion
{
miriam-gene:2244
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN584406820685107556f40a7b81b67542
sio:SIO_000628
miriam-gene:2244
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP44065.RATjQbmcE9pxUDRspkXnlCUN_GCyWNsBvyhmvGvi-Hqvk130_provenance
{
dgn-np:NP44065.RATjQbmcE9pxUDRspkXnlCUN_GCyWNsBvyhmvGvi-Hqvk130_assertion
dcterms:description
"[ These data suggest a relationship between the -455 G/A beta-fibrinogen gene polymorphism and the development of CAD in subjects with NIDDM. This relationship was not associated with variations in fibrinogen levels, suggesting that this polymorphism may be in linkage with a polymorphism within the coding region of the beta-fibrinogen gene, which results in an alteration in the stability of the fibrin clot.]. 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:8908392
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP44065.RATjQbmcE9pxUDRspkXnlCUN_GCyWNsBvyhmvGvi-Hqvk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}