@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44573.RAYma1sMpnfCOlxFQnhEiMXKcpn62VN5IkT55T9ckStcA
> .
@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:NP44573.RAYma1sMpnfCOlxFQnhEiMXKcpn62VN5IkT55T9ckStcA130_head
{
this:
np:hasAssertion
dgn-np:NP44573.RAYma1sMpnfCOlxFQnhEiMXKcpn62VN5IkT55T9ckStcA130_assertion
;
np:hasProvenance
dgn-np:NP44573.RAYma1sMpnfCOlxFQnhEiMXKcpn62VN5IkT55T9ckStcA130_provenance
;
np:hasPublicationInfo
dgn-np:NP44573.RAYma1sMpnfCOlxFQnhEiMXKcpn62VN5IkT55T9ckStcA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44573.RAYma1sMpnfCOlxFQnhEiMXKcpn62VN5IkT55T9ckStcA130_assertion
a
np:Assertion
.
dgn-np:NP44573.RAYma1sMpnfCOlxFQnhEiMXKcpn62VN5IkT55T9ckStcA130_provenance
a
np:Provenance
.
dgn-np:NP44573.RAYma1sMpnfCOlxFQnhEiMXKcpn62VN5IkT55T9ckStcA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44573.RAYma1sMpnfCOlxFQnhEiMXKcpn62VN5IkT55T9ckStcA130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN85fb5b6fe864191557f959e5d8bfa16d
sio:SIO_000628
miriam-gene:2147
,
lld:C1956346
;
a
sio:SIO_001122
.
}
dgn-np:NP44573.RAYma1sMpnfCOlxFQnhEiMXKcpn62VN5IkT55T9ckStcA130_provenance
{
dgn-np:NP44573.RAYma1sMpnfCOlxFQnhEiMXKcpn62VN5IkT55T9ckStcA130_assertion
dcterms:description
"[Although both the heterozygote Factor VLeiden and Prothrombin gene mutations were more frequent in patients with CAD than in control subjects, there was no statistical relationship found to exist between coronary artery disease and the Factor VLeiden and Prothrombin G20210A mutations.]. 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:18452260
;
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:NP44573.RAYma1sMpnfCOlxFQnhEiMXKcpn62VN5IkT55T9ckStcA130_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" .
}