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http://rdf.disgenet.org/nanopublications.trig#NP51893.RA8X_y0JOnVc9EWAwcmVrhcG-ccbA3xgZzPYUICCVMlz4
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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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#
> .
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{
this:
np:hasAssertion
dgn-np:NP51893.RA8X_y0JOnVc9EWAwcmVrhcG-ccbA3xgZzPYUICCVMlz4130_assertion
;
np:hasProvenance
dgn-np:NP51893.RA8X_y0JOnVc9EWAwcmVrhcG-ccbA3xgZzPYUICCVMlz4130_provenance
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np:hasPublicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP51893.RA8X_y0JOnVc9EWAwcmVrhcG-ccbA3xgZzPYUICCVMlz4130_provenance
a
np:Provenance
.
dgn-np:NP51893.RA8X_y0JOnVc9EWAwcmVrhcG-ccbA3xgZzPYUICCVMlz4130_publicationInfo
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dgn-np:NP51893.RA8X_y0JOnVc9EWAwcmVrhcG-ccbA3xgZzPYUICCVMlz4130_assertion
{
miriam-gene:5054
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNe354ce7f79b76c1cd967d9cd54f52f15
sio:SIO_000628
miriam-gene:5054
,
lld:C0020538
;
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.
}
dgn-np:NP51893.RA8X_y0JOnVc9EWAwcmVrhcG-ccbA3xgZzPYUICCVMlz4130_provenance
{
dgn-np:NP51893.RA8X_y0JOnVc9EWAwcmVrhcG-ccbA3xgZzPYUICCVMlz4130_assertion
dcterms:description
"[Genomic DNA was isolated from 214 CTEPH subjects and 200 healthy controls, and analysed for Factor V Leiden, prothrombin guanine (G) to adenine (A) substitution at nucleotide 20210 (20210G>A), plasminogen activator inhibitor-1 4G/5G, tissue plasminogen activator 7351 cytosine (C)>thymidine (T), Factor XIII 100G>T, fibrinogen Aalpha substitution of threonine with alanine at position 312 (Thr312Ala), fibrinogen Bbeta substitution of arginine with lysine at position 448 (Arg448Lys) and fibrinogen Bbeta 455G>A polymorphisms.]. 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:18057060
;
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:NP51893.RA8X_y0JOnVc9EWAwcmVrhcG-ccbA3xgZzPYUICCVMlz4130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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pav:authoredBy
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> , <
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> ;
pav:createdBy
<
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pav:version
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}