@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP729701.RADbt9NLL4IMfxgIO_I5HSHqGA4-oZL-qNOMrx-2ywGxo
> .
@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/v4.0.0/void/
> .
dgn-np:NP729701.RADbt9NLL4IMfxgIO_I5HSHqGA4-oZL-qNOMrx-2ywGxo130_head
{
this:
np:hasAssertion
dgn-np:NP729701.RADbt9NLL4IMfxgIO_I5HSHqGA4-oZL-qNOMrx-2ywGxo130_assertion
;
np:hasProvenance
dgn-np:NP729701.RADbt9NLL4IMfxgIO_I5HSHqGA4-oZL-qNOMrx-2ywGxo130_provenance
;
np:hasPublicationInfo
dgn-np:NP729701.RADbt9NLL4IMfxgIO_I5HSHqGA4-oZL-qNOMrx-2ywGxo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP729701.RADbt9NLL4IMfxgIO_I5HSHqGA4-oZL-qNOMrx-2ywGxo130_assertion
a
np:Assertion
.
dgn-np:NP729701.RADbt9NLL4IMfxgIO_I5HSHqGA4-oZL-qNOMrx-2ywGxo130_provenance
a
np:Provenance
.
dgn-np:NP729701.RADbt9NLL4IMfxgIO_I5HSHqGA4-oZL-qNOMrx-2ywGxo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP729701.RADbt9NLL4IMfxgIO_I5HSHqGA4-oZL-qNOMrx-2ywGxo130_assertion
{
miriam-gene:3674
a
ncit:C16612
.
lld:C0040015
a
ncit:C7057
.
dgn-gda:DGN2e075f312ac630f5f6eec0bca8e058a2
sio:SIO_000628
miriam-gene:3674
,
lld:C0040015
;
a
sio:SIO_001121
.
}
dgn-np:NP729701.RADbt9NLL4IMfxgIO_I5HSHqGA4-oZL-qNOMrx-2ywGxo130_provenance
{
dgn-np:NP729701.RADbt9NLL4IMfxgIO_I5HSHqGA4-oZL-qNOMrx-2ywGxo130_assertion
dcterms:description
"[Defects of integrin alpha(IIb)beta(3) are typical of Glanzmann's thrombasthenia, an inherited autosomal recessive bleeding disorder characterized by the failure of platelets to aggregate in response to all physiological agonists, but with no abnormalities in the number or size of platelets.]. 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:19336737
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP729701.RADbt9NLL4IMfxgIO_I5HSHqGA4-oZL-qNOMrx-2ywGxo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:16+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}