@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP939689.RA6FxG6OW2ZnD9VTdJYO-63EGMPFW-Agc91A07SKI78_M
> .
@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:NP939689.RA6FxG6OW2ZnD9VTdJYO-63EGMPFW-Agc91A07SKI78_M130_head
{
this:
np:hasAssertion
dgn-np:NP939689.RA6FxG6OW2ZnD9VTdJYO-63EGMPFW-Agc91A07SKI78_M130_assertion
;
np:hasProvenance
dgn-np:NP939689.RA6FxG6OW2ZnD9VTdJYO-63EGMPFW-Agc91A07SKI78_M130_provenance
;
np:hasPublicationInfo
dgn-np:NP939689.RA6FxG6OW2ZnD9VTdJYO-63EGMPFW-Agc91A07SKI78_M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP939689.RA6FxG6OW2ZnD9VTdJYO-63EGMPFW-Agc91A07SKI78_M130_assertion
a
np:Assertion
.
dgn-np:NP939689.RA6FxG6OW2ZnD9VTdJYO-63EGMPFW-Agc91A07SKI78_M130_provenance
a
np:Provenance
.
dgn-np:NP939689.RA6FxG6OW2ZnD9VTdJYO-63EGMPFW-Agc91A07SKI78_M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP939689.RA6FxG6OW2ZnD9VTdJYO-63EGMPFW-Agc91A07SKI78_M130_assertion
{
miriam-gene:11093
a
ncit:C16612
.
lld:C0857305
a
ncit:C7057
.
dgn-gda:DGN2291858da4d8edd2cacb28236df1e3a7
sio:SIO_000628
miriam-gene:11093
,
lld:C0857305
;
a
sio:SIO_001121
.
}
dgn-np:NP939689.RA6FxG6OW2ZnD9VTdJYO-63EGMPFW-Agc91A07SKI78_M130_provenance
{
dgn-np:NP939689.RA6FxG6OW2ZnD9VTdJYO-63EGMPFW-Agc91A07SKI78_M130_assertion
dcterms:description
"[The recent discovery of the von Willebrand Factor (vWF) cleaving protease (ADAMTS13) and the association of its deficiency with thrombotic thrombocytopaenic purpura (TTP) has generated both enormous interest and considerable confusion.]. 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:12656756
;
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:NP939689.RA6FxG6OW2ZnD9VTdJYO-63EGMPFW-Agc91A07SKI78_M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}