@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP339220.RAjKL3i908bFWR8qoeimrUOMnqCYFC2PiOJoHbtEaxLKc
> .
@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:NP339220.RAjKL3i908bFWR8qoeimrUOMnqCYFC2PiOJoHbtEaxLKc130_head
{
this:
np:hasAssertion
dgn-np:NP339220.RAjKL3i908bFWR8qoeimrUOMnqCYFC2PiOJoHbtEaxLKc130_assertion
;
np:hasProvenance
dgn-np:NP339220.RAjKL3i908bFWR8qoeimrUOMnqCYFC2PiOJoHbtEaxLKc130_provenance
;
np:hasPublicationInfo
dgn-np:NP339220.RAjKL3i908bFWR8qoeimrUOMnqCYFC2PiOJoHbtEaxLKc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP339220.RAjKL3i908bFWR8qoeimrUOMnqCYFC2PiOJoHbtEaxLKc130_assertion
a
np:Assertion
.
dgn-np:NP339220.RAjKL3i908bFWR8qoeimrUOMnqCYFC2PiOJoHbtEaxLKc130_provenance
a
np:Provenance
.
dgn-np:NP339220.RAjKL3i908bFWR8qoeimrUOMnqCYFC2PiOJoHbtEaxLKc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP339220.RAjKL3i908bFWR8qoeimrUOMnqCYFC2PiOJoHbtEaxLKc130_assertion
{
miriam-gene:7450
a
ncit:C16612
.
lld:C0034155
a
ncit:C7057
.
dgn-gda:DGN419507d97658408b81fc311752edf73f
sio:SIO_000628
miriam-gene:7450
,
lld:C0034155
;
a
sio:SIO_001121
.
}
dgn-np:NP339220.RAjKL3i908bFWR8qoeimrUOMnqCYFC2PiOJoHbtEaxLKc130_provenance
{
dgn-np:NP339220.RAjKL3i908bFWR8qoeimrUOMnqCYFC2PiOJoHbtEaxLKc130_assertion
dcterms:description
"[The etiology of TTP is mainly due to insufficient cleavage of the large multimers of von Willebrand factor (vWF) secondary to decreased activity of ADAMTS13 (a disintegrin and metalloprotease with Thrombospondin type 1 repeats, member 13).]. 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:23146723
;
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:NP339220.RAjKL3i908bFWR8qoeimrUOMnqCYFC2PiOJoHbtEaxLKc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:19+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" .
}