@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1280202.RAbRE7ne7as3iupspvIViMMAqut9pU7HKi2ww1IzcEeOE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1280202.RAbRE7ne7as3iupspvIViMMAqut9pU7HKi2ww1IzcEeOE130_head
{
this:
np:hasAssertion
dgn-np:NP1280202.RAbRE7ne7as3iupspvIViMMAqut9pU7HKi2ww1IzcEeOE130_assertion
;
np:hasProvenance
dgn-np:NP1280202.RAbRE7ne7as3iupspvIViMMAqut9pU7HKi2ww1IzcEeOE130_provenance
;
np:hasPublicationInfo
dgn-np:NP1280202.RAbRE7ne7as3iupspvIViMMAqut9pU7HKi2ww1IzcEeOE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1280202.RAbRE7ne7as3iupspvIViMMAqut9pU7HKi2ww1IzcEeOE130_assertion
a
np:Assertion
.
dgn-np:NP1280202.RAbRE7ne7as3iupspvIViMMAqut9pU7HKi2ww1IzcEeOE130_provenance
a
np:Provenance
.
dgn-np:NP1280202.RAbRE7ne7as3iupspvIViMMAqut9pU7HKi2ww1IzcEeOE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1280202.RAbRE7ne7as3iupspvIViMMAqut9pU7HKi2ww1IzcEeOE130_assertion
{
miriam-gene:7450
a
ncit:C16612
.
lld:C0042974
a
ncit:C7057
.
dgn-gda:DGNf30ec895af2e4c567369aea3ac16a39f
sio:SIO_000628
miriam-gene:7450
,
lld:C0042974
;
a
sio:SIO_001121
.
}
dgn-np:NP1280202.RAbRE7ne7as3iupspvIViMMAqut9pU7HKi2ww1IzcEeOE130_provenance
{
dgn-np:NP1280202.RAbRE7ne7as3iupspvIViMMAqut9pU7HKi2ww1IzcEeOE130_assertion
dcterms:description
"[The von Willebrand disease (VWD) phenotype of the patient featured low plasma and platelet VWF, multimers with smears extending over the highest normal oligomers in plasma, but not platelets, and an impaired collagen-binding capacity.]. 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:25904363
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1280202.RAbRE7ne7as3iupspvIViMMAqut9pU7HKi2ww1IzcEeOE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:26+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}