@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y
> .
@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:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_head
{
this:
np:hasAssertion
dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_assertion
;
np:hasProvenance
dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_assertion
a
np:Assertion
.
dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_provenance
a
np:Provenance
.
dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_assertion
{
miriam-gene:3674
a
ncit:C16612
.
lld:C0005129
a
ncit:C7057
.
dgn-gda:DGN01d37bcceab462114ffb0b0771fadca7
sio:SIO_000628
miriam-gene:3674
,
lld:C0005129
;
a
sio:SIO_001121
.
}
dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_provenance
{
dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_assertion
dcterms:description
"[While encountered only rarely, carriers of either GT or Bernard Soulier syndrome that are at the same time heterozygous for human platelet alloantigenic epitopes found on GPIb, GPIIb, or GPIIIa have the possibility to give discrepant results when comparing genotypic versus phenotypic analysis.]. 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:8916947
;
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:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:03+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" .
}