@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP746411.RABqKxWDhe1sEPlpbjpOnCvCXkFm901PC-3zhHQWvDYUg
> .
@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:NP746411.RABqKxWDhe1sEPlpbjpOnCvCXkFm901PC-3zhHQWvDYUg130_head
{
this:
np:hasAssertion
dgn-np:NP746411.RABqKxWDhe1sEPlpbjpOnCvCXkFm901PC-3zhHQWvDYUg130_assertion
;
np:hasProvenance
dgn-np:NP746411.RABqKxWDhe1sEPlpbjpOnCvCXkFm901PC-3zhHQWvDYUg130_provenance
;
np:hasPublicationInfo
dgn-np:NP746411.RABqKxWDhe1sEPlpbjpOnCvCXkFm901PC-3zhHQWvDYUg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP746411.RABqKxWDhe1sEPlpbjpOnCvCXkFm901PC-3zhHQWvDYUg130_assertion
a
np:Assertion
.
dgn-np:NP746411.RABqKxWDhe1sEPlpbjpOnCvCXkFm901PC-3zhHQWvDYUg130_provenance
a
np:Provenance
.
dgn-np:NP746411.RABqKxWDhe1sEPlpbjpOnCvCXkFm901PC-3zhHQWvDYUg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP746411.RABqKxWDhe1sEPlpbjpOnCvCXkFm901PC-3zhHQWvDYUg130_assertion
{
miriam-gene:5319
a
ncit:C16612
.
lld:C1868251
a
ncit:C7057
.
dgn-gda:DGN005abc062c06c2f6d95af2d7edf4e935
sio:SIO_000628
miriam-gene:5319
,
lld:C1868251
;
a
sio:SIO_001121
.
}
dgn-np:NP746411.RABqKxWDhe1sEPlpbjpOnCvCXkFm901PC-3zhHQWvDYUg130_provenance
{
dgn-np:NP746411.RABqKxWDhe1sEPlpbjpOnCvCXkFm901PC-3zhHQWvDYUg130_assertion
dcterms:description
"[The platelet antigens, PlA1 and PlA2, are responsible for most cases of posttransfusion purpura (PTP) and neonatal alloimmune thrombocytopenia (NAIT) in the caucasian population and are determined by two allelic forms of the platelet glycoprotein GPIIIa gene.]. 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:7519475
;
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:NP746411.RABqKxWDhe1sEPlpbjpOnCvCXkFm901PC-3zhHQWvDYUg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:32+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" .
}