@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP509266.RAQbXZ1ZVK9KitN97GbrnS8Fq9KHniWdqkJWGOWYGXNVo
> .
@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:NP509266.RAQbXZ1ZVK9KitN97GbrnS8Fq9KHniWdqkJWGOWYGXNVo130_head
{
this:
np:hasAssertion
dgn-np:NP509266.RAQbXZ1ZVK9KitN97GbrnS8Fq9KHniWdqkJWGOWYGXNVo130_assertion
;
np:hasProvenance
dgn-np:NP509266.RAQbXZ1ZVK9KitN97GbrnS8Fq9KHniWdqkJWGOWYGXNVo130_provenance
;
np:hasPublicationInfo
dgn-np:NP509266.RAQbXZ1ZVK9KitN97GbrnS8Fq9KHniWdqkJWGOWYGXNVo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP509266.RAQbXZ1ZVK9KitN97GbrnS8Fq9KHniWdqkJWGOWYGXNVo130_assertion
a
np:Assertion
.
dgn-np:NP509266.RAQbXZ1ZVK9KitN97GbrnS8Fq9KHniWdqkJWGOWYGXNVo130_provenance
a
np:Provenance
.
dgn-np:NP509266.RAQbXZ1ZVK9KitN97GbrnS8Fq9KHniWdqkJWGOWYGXNVo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP509266.RAQbXZ1ZVK9KitN97GbrnS8Fq9KHniWdqkJWGOWYGXNVo130_assertion
{
miriam-gene:5555
a
ncit:C16612
.
lld:C0018799
a
ncit:C7057
.
dgn-gda:DGNb2bb47d81517977d62ba35c0e52c661d
sio:SIO_000628
miriam-gene:5555
,
lld:C0018799
;
a
sio:SIO_001121
.
}
dgn-np:NP509266.RAQbXZ1ZVK9KitN97GbrnS8Fq9KHniWdqkJWGOWYGXNVo130_provenance
{
dgn-np:NP509266.RAQbXZ1ZVK9KitN97GbrnS8Fq9KHniWdqkJWGOWYGXNVo130_assertion
dcterms:description
"[They include cardiac disease, vascular abnormalities, endothelial damage, infectious diseases, collagen tissue diseases, certain inborn errors of metabolism and anticardiolipin antibody, lupus anticoagulant and deficiencies of protein C, protein S, antithrombin or plasminogen.]. 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:19432826
;
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:NP509266.RAQbXZ1ZVK9KitN97GbrnS8Fq9KHniWdqkJWGOWYGXNVo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:03+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" .
}