@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP992043.RAI4jJMqOYQ5AH4YcUHXJMDlOAMiFzs7XIBBO83KLTThY
> .
@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:NP992043.RAI4jJMqOYQ5AH4YcUHXJMDlOAMiFzs7XIBBO83KLTThY130_head
{
this:
np:hasAssertion
dgn-np:NP992043.RAI4jJMqOYQ5AH4YcUHXJMDlOAMiFzs7XIBBO83KLTThY130_assertion
;
np:hasProvenance
dgn-np:NP992043.RAI4jJMqOYQ5AH4YcUHXJMDlOAMiFzs7XIBBO83KLTThY130_provenance
;
np:hasPublicationInfo
dgn-np:NP992043.RAI4jJMqOYQ5AH4YcUHXJMDlOAMiFzs7XIBBO83KLTThY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP992043.RAI4jJMqOYQ5AH4YcUHXJMDlOAMiFzs7XIBBO83KLTThY130_assertion
a
np:Assertion
.
dgn-np:NP992043.RAI4jJMqOYQ5AH4YcUHXJMDlOAMiFzs7XIBBO83KLTThY130_provenance
a
np:Provenance
.
dgn-np:NP992043.RAI4jJMqOYQ5AH4YcUHXJMDlOAMiFzs7XIBBO83KLTThY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP992043.RAI4jJMqOYQ5AH4YcUHXJMDlOAMiFzs7XIBBO83KLTThY130_assertion
{
miriam-gene:7450
a
ncit:C16612
.
lld:C1264041
a
ncit:C7057
.
dgn-gda:DGN8e09c59daccc8ea642075660f071ac07
sio:SIO_000628
miriam-gene:7450
,
lld:C1264041
;
a
sio:SIO_001121
.
}
dgn-np:NP992043.RAI4jJMqOYQ5AH4YcUHXJMDlOAMiFzs7XIBBO83KLTThY130_provenance
{
dgn-np:NP992043.RAI4jJMqOYQ5AH4YcUHXJMDlOAMiFzs7XIBBO83KLTThY130_assertion
dcterms:description
"[Although the incidence of VWD3 is rare, the condition is of considerable interest because of its severe clinical presentation, the need for replacement therapy and the risk of alloantibodies following infusion of plasma-derived VWF concentrates.]. 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:22722677
;
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:NP992043.RAI4jJMqOYQ5AH4YcUHXJMDlOAMiFzs7XIBBO83KLTThY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:15+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" .
}