@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM
> .
@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:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_head
{
this:
np:hasAssertion
dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_assertion
;
np:hasProvenance
dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_provenance
;
np:hasPublicationInfo
dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_assertion
a
np:Assertion
.
dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_provenance
a
np:Provenance
.
dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_assertion
{
miriam-gene:1351
a
ncit:C16612
.
lld:C2827470
a
ncit:C7057
.
dgn-gda:DGN823c8bc3627d6666d0f91e403173755a
sio:SIO_000628
miriam-gene:1351
,
lld:C2827470
;
a
sio:SIO_001121
.
}
dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_provenance
{
dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_assertion
dcterms:description
"[Thrombophilia was suspected and the relative investigation revealed high levels of factor VIII procoagulant, which is frequent in hemodialysis patients, and resistance to activated protein C. Polymerase chain reaction detected that the patient was heterozygous for factor V Leiden, which is quite common in general population.]. 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:18387172
;
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:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:46+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" .
}