@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP263912.RAHiKQSIQzoiVzUPtG4YcZAvIDvhqh0I5flHPqgDOr4WM
> .
@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:NP263912.RAHiKQSIQzoiVzUPtG4YcZAvIDvhqh0I5flHPqgDOr4WM130_head
{
this:
np:hasAssertion
dgn-np:NP263912.RAHiKQSIQzoiVzUPtG4YcZAvIDvhqh0I5flHPqgDOr4WM130_assertion
;
np:hasProvenance
dgn-np:NP263912.RAHiKQSIQzoiVzUPtG4YcZAvIDvhqh0I5flHPqgDOr4WM130_provenance
;
np:hasPublicationInfo
dgn-np:NP263912.RAHiKQSIQzoiVzUPtG4YcZAvIDvhqh0I5flHPqgDOr4WM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP263912.RAHiKQSIQzoiVzUPtG4YcZAvIDvhqh0I5flHPqgDOr4WM130_assertion
a
np:Assertion
.
dgn-np:NP263912.RAHiKQSIQzoiVzUPtG4YcZAvIDvhqh0I5flHPqgDOr4WM130_provenance
a
np:Provenance
.
dgn-np:NP263912.RAHiKQSIQzoiVzUPtG4YcZAvIDvhqh0I5flHPqgDOr4WM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP263912.RAHiKQSIQzoiVzUPtG4YcZAvIDvhqh0I5flHPqgDOr4WM130_assertion
{
miriam-gene:7450
a
ncit:C16612
.
lld:C1282971
a
ncit:C7057
.
dgn-gda:DGNcaa736dcb30532680a8bbd19528d886b
sio:SIO_000628
miriam-gene:7450
,
lld:C1282971
;
a
sio:SIO_001121
.
}
dgn-np:NP263912.RAHiKQSIQzoiVzUPtG4YcZAvIDvhqh0I5flHPqgDOr4WM130_provenance
{
dgn-np:NP263912.RAHiKQSIQzoiVzUPtG4YcZAvIDvhqh0I5flHPqgDOr4WM130_assertion
dcterms:description
"[Type 2B von Willebrand disease (vWD) is characterized by the absence of the very high molecular weight von Willebrand factor (vWF) multimers from plasma, which is caused by spontaneous binding to platelet receptor glycoprotein Ib (GPIb).]. 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:9108394
;
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:NP263912.RAHiKQSIQzoiVzUPtG4YcZAvIDvhqh0I5flHPqgDOr4WM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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" .
}