@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP513875.RAYahVTGLb36GYL-2FWbGdBTk20DQHBT6HuotrQClxgsM
> .
@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:NP513875.RAYahVTGLb36GYL-2FWbGdBTk20DQHBT6HuotrQClxgsM130_head
{
this:
np:hasAssertion
dgn-np:NP513875.RAYahVTGLb36GYL-2FWbGdBTk20DQHBT6HuotrQClxgsM130_assertion
;
np:hasProvenance
dgn-np:NP513875.RAYahVTGLb36GYL-2FWbGdBTk20DQHBT6HuotrQClxgsM130_provenance
;
np:hasPublicationInfo
dgn-np:NP513875.RAYahVTGLb36GYL-2FWbGdBTk20DQHBT6HuotrQClxgsM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP513875.RAYahVTGLb36GYL-2FWbGdBTk20DQHBT6HuotrQClxgsM130_assertion
a
np:Assertion
.
dgn-np:NP513875.RAYahVTGLb36GYL-2FWbGdBTk20DQHBT6HuotrQClxgsM130_provenance
a
np:Provenance
.
dgn-np:NP513875.RAYahVTGLb36GYL-2FWbGdBTk20DQHBT6HuotrQClxgsM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP513875.RAYahVTGLb36GYL-2FWbGdBTk20DQHBT6HuotrQClxgsM130_assertion
{
miriam-gene:22915
a
ncit:C16612
.
lld:C1866423
a
ncit:C7057
.
dgn-gda:DGNde91c5895d2c99fc801c031b67790e36
sio:SIO_000628
miriam-gene:22915
,
lld:C1866423
;
a
sio:SIO_001121
.
}
dgn-np:NP513875.RAYahVTGLb36GYL-2FWbGdBTk20DQHBT6HuotrQClxgsM130_provenance
{
dgn-np:NP513875.RAYahVTGLb36GYL-2FWbGdBTk20DQHBT6HuotrQClxgsM130_assertion
dcterms:description
"[These data indicate that patients with factor V Quebec have an inherited bleeding disorder distinct from other platelet disorders and associated with multiple abnormalities, including multimerin deficiency, abnormal platelet factor V, thrombospondin, von Willebrand factor, and fibrinogen, and an epinephrine aggregation defect.]. 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:8652809
;
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:NP513875.RAYahVTGLb36GYL-2FWbGdBTk20DQHBT6HuotrQClxgsM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:06+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" .
}