@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP836313.RAGEwYXXpsQYifrdgLnDB18BhJ6GjSbcjmE5D8R8vdii4
> .
@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:NP836313.RAGEwYXXpsQYifrdgLnDB18BhJ6GjSbcjmE5D8R8vdii4130_head
{
this:
np:hasAssertion
dgn-np:NP836313.RAGEwYXXpsQYifrdgLnDB18BhJ6GjSbcjmE5D8R8vdii4130_assertion
;
np:hasProvenance
dgn-np:NP836313.RAGEwYXXpsQYifrdgLnDB18BhJ6GjSbcjmE5D8R8vdii4130_provenance
;
np:hasPublicationInfo
dgn-np:NP836313.RAGEwYXXpsQYifrdgLnDB18BhJ6GjSbcjmE5D8R8vdii4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP836313.RAGEwYXXpsQYifrdgLnDB18BhJ6GjSbcjmE5D8R8vdii4130_assertion
a
np:Assertion
.
dgn-np:NP836313.RAGEwYXXpsQYifrdgLnDB18BhJ6GjSbcjmE5D8R8vdii4130_provenance
a
np:Provenance
.
dgn-np:NP836313.RAGEwYXXpsQYifrdgLnDB18BhJ6GjSbcjmE5D8R8vdii4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP836313.RAGEwYXXpsQYifrdgLnDB18BhJ6GjSbcjmE5D8R8vdii4130_assertion
{
miriam-gene:11093
a
ncit:C16612
.
lld:C0002871
a
ncit:C7057
.
dgn-gda:DGN59a1b8daf3f653cca175862b3563cbcb
sio:SIO_000628
miriam-gene:11093
,
lld:C0002871
;
a
sio:SIO_001121
.
}
dgn-np:NP836313.RAGEwYXXpsQYifrdgLnDB18BhJ6GjSbcjmE5D8R8vdii4130_provenance
{
dgn-np:NP836313.RAGEwYXXpsQYifrdgLnDB18BhJ6GjSbcjmE5D8R8vdii4130_assertion
dcterms:description
"[Here we report on a girl who presented with recurrent thrombocytopenia and anaemia since birth, developing the full pentad of characteristic TTP at the age of 16 y. Congenital TTP was confirmed on the basis of severe VWF-CP deficiency in the absence of an acquired inhibitor.]. 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:12434890
;
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:NP836313.RAGEwYXXpsQYifrdgLnDB18BhJ6GjSbcjmE5D8R8vdii4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:31+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" .
}