@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP175144.RACAAOKYSp_5sN8WI-DVBjnCOZiN1a08DV7OkshSmwQx4
> .
@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 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:NP175144.RACAAOKYSp_5sN8WI-DVBjnCOZiN1a08DV7OkshSmwQx4130_head
{
this:
np:hasAssertion
dgn-np:NP175144.RACAAOKYSp_5sN8WI-DVBjnCOZiN1a08DV7OkshSmwQx4130_assertion
;
np:hasProvenance
dgn-np:NP175144.RACAAOKYSp_5sN8WI-DVBjnCOZiN1a08DV7OkshSmwQx4130_provenance
;
np:hasPublicationInfo
dgn-np:NP175144.RACAAOKYSp_5sN8WI-DVBjnCOZiN1a08DV7OkshSmwQx4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP175144.RACAAOKYSp_5sN8WI-DVBjnCOZiN1a08DV7OkshSmwQx4130_assertion
a
np:Assertion
.
dgn-np:NP175144.RACAAOKYSp_5sN8WI-DVBjnCOZiN1a08DV7OkshSmwQx4130_provenance
a
np:Provenance
.
dgn-np:NP175144.RACAAOKYSp_5sN8WI-DVBjnCOZiN1a08DV7OkshSmwQx4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP175144.RACAAOKYSp_5sN8WI-DVBjnCOZiN1a08DV7OkshSmwQx4130_assertion
{
miriam-gene:27319
a
ncit:C16612
.
lld:C0040015
a
ncit:C7057
.
dgn-gda:DGN569a59c705ad373319f92a3c3f9efb1a
sio:SIO_000628
miriam-gene:27319
,
lld:C0040015
;
a
sio:SIO_001121
.
}
dgn-np:NP175144.RACAAOKYSp_5sN8WI-DVBjnCOZiN1a08DV7OkshSmwQx4130_provenance
{
dgn-np:NP175144.RACAAOKYSp_5sN8WI-DVBjnCOZiN1a08DV7OkshSmwQx4130_assertion
dct:description
"[We have been studying two populations having an unusually high frequency of Glanzmann disease, Iraqi Jews and Arabs living in Israel, and were able to distinguish the populations on the basis of immunodetectable GPIIIa and platelet surface vitronectin receptor (alpha v beta 3) expression.]. 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:2014236
;
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:NP175144.RACAAOKYSp_5sN8WI-DVBjnCOZiN1a08DV7OkshSmwQx4130_publicationInfo
{
this:
dct:created
"2014-10-02T12:33:34+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}