@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP616005.RAFmuDbR8ALXqr0xPyifbD-Z7rqLqPaoY4HYyqQC2wC9s
> .
@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:NP616005.RAFmuDbR8ALXqr0xPyifbD-Z7rqLqPaoY4HYyqQC2wC9s130_head
{
this:
np:hasAssertion
dgn-np:NP616005.RAFmuDbR8ALXqr0xPyifbD-Z7rqLqPaoY4HYyqQC2wC9s130_assertion
;
np:hasProvenance
dgn-np:NP616005.RAFmuDbR8ALXqr0xPyifbD-Z7rqLqPaoY4HYyqQC2wC9s130_provenance
;
np:hasPublicationInfo
dgn-np:NP616005.RAFmuDbR8ALXqr0xPyifbD-Z7rqLqPaoY4HYyqQC2wC9s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP616005.RAFmuDbR8ALXqr0xPyifbD-Z7rqLqPaoY4HYyqQC2wC9s130_assertion
a
np:Assertion
.
dgn-np:NP616005.RAFmuDbR8ALXqr0xPyifbD-Z7rqLqPaoY4HYyqQC2wC9s130_provenance
a
np:Provenance
.
dgn-np:NP616005.RAFmuDbR8ALXqr0xPyifbD-Z7rqLqPaoY4HYyqQC2wC9s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP616005.RAFmuDbR8ALXqr0xPyifbD-Z7rqLqPaoY4HYyqQC2wC9s130_assertion
{
miriam-gene:11093
a
ncit:C16612
.
lld:C0162429
a
ncit:C7057
.
dgn-gda:DGNfc76fa22682746a359f04996be6b69d8
sio:SIO_000628
miriam-gene:11093
,
lld:C0162429
;
a
sio:SIO_001121
.
}
dgn-np:NP616005.RAFmuDbR8ALXqr0xPyifbD-Z7rqLqPaoY4HYyqQC2wC9s130_provenance
{
dgn-np:NP616005.RAFmuDbR8ALXqr0xPyifbD-Z7rqLqPaoY4HYyqQC2wC9s130_assertion
dcterms:description
"[The physiopathology of thrombotic thrombocytopenic purpura (TTP) has been clarified since 1998, when it was shown that TTP in adults was most often associated with an acquired deficiency of von Willebrand factor-cleaving protease (ADAMTS13) due to autoantibodies, whereas TTP in children was most often associated with a hereditary autosomal recessive severe deficiency of ADAMTS13.]. 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:16575683
;
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:NP616005.RAFmuDbR8ALXqr0xPyifbD-Z7rqLqPaoY4HYyqQC2wC9s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:12+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" .
}