@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP859877.RATYgqlhhWmBsukzVvWOAZ6K7g37oj0hcGxpeuxrnGKAM
> .
@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/v3.0.0/void/
> .
dgn-np:NP859877.RATYgqlhhWmBsukzVvWOAZ6K7g37oj0hcGxpeuxrnGKAM130_head
{
this:
np:hasAssertion
dgn-np:NP859877.RATYgqlhhWmBsukzVvWOAZ6K7g37oj0hcGxpeuxrnGKAM130_assertion
;
np:hasProvenance
dgn-np:NP859877.RATYgqlhhWmBsukzVvWOAZ6K7g37oj0hcGxpeuxrnGKAM130_provenance
;
np:hasPublicationInfo
dgn-np:NP859877.RATYgqlhhWmBsukzVvWOAZ6K7g37oj0hcGxpeuxrnGKAM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP859877.RATYgqlhhWmBsukzVvWOAZ6K7g37oj0hcGxpeuxrnGKAM130_assertion
a
np:Assertion
.
dgn-np:NP859877.RATYgqlhhWmBsukzVvWOAZ6K7g37oj0hcGxpeuxrnGKAM130_provenance
a
np:Provenance
.
dgn-np:NP859877.RATYgqlhhWmBsukzVvWOAZ6K7g37oj0hcGxpeuxrnGKAM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP859877.RATYgqlhhWmBsukzVvWOAZ6K7g37oj0hcGxpeuxrnGKAM130_assertion
{
miriam-gene:11093
a
ncit:C16612
.
lld:C1268935
a
ncit:C7057
.
dgn-gda:DGN5475d164ad10a24c1d318fbcc9c8ea54
sio:SIO_000628
miriam-gene:11093
,
lld:C1268935
;
a
sio:SIO_001121
.
}
dgn-np:NP859877.RATYgqlhhWmBsukzVvWOAZ6K7g37oj0hcGxpeuxrnGKAM130_provenance
{
dgn-np:NP859877.RATYgqlhhWmBsukzVvWOAZ6K7g37oj0hcGxpeuxrnGKAM130_assertion
dcterms:description
"[Congenital thrombotic thrombocytopenic purpura (TTP) is an inherited disease caused by mutations in the ADAMTS 13 gene and has been reported to have diverse ages of presentation, ranging from the newborn period to adulthood.]. 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:24115559
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP859877.RATYgqlhhWmBsukzVvWOAZ6K7g37oj0hcGxpeuxrnGKAM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:22+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}