@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP55774.RATFbLZ0l8QSBvAP7oLxPi_bJYF667ZE5Io7gJaF6q2ug
> .
@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:NP55774.RATFbLZ0l8QSBvAP7oLxPi_bJYF667ZE5Io7gJaF6q2ug130_head
{
this:
np:hasAssertion
dgn-np:NP55774.RATFbLZ0l8QSBvAP7oLxPi_bJYF667ZE5Io7gJaF6q2ug130_assertion
;
np:hasProvenance
dgn-np:NP55774.RATFbLZ0l8QSBvAP7oLxPi_bJYF667ZE5Io7gJaF6q2ug130_provenance
;
np:hasPublicationInfo
dgn-np:NP55774.RATFbLZ0l8QSBvAP7oLxPi_bJYF667ZE5Io7gJaF6q2ug130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55774.RATFbLZ0l8QSBvAP7oLxPi_bJYF667ZE5Io7gJaF6q2ug130_assertion
a
np:Assertion
.
dgn-np:NP55774.RATFbLZ0l8QSBvAP7oLxPi_bJYF667ZE5Io7gJaF6q2ug130_provenance
a
np:Provenance
.
dgn-np:NP55774.RATFbLZ0l8QSBvAP7oLxPi_bJYF667ZE5Io7gJaF6q2ug130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55774.RATFbLZ0l8QSBvAP7oLxPi_bJYF667ZE5Io7gJaF6q2ug130_assertion
{
miriam-gene:3673
a
ncit:C16612
.
lld:C0004943
a
ncit:C7057
.
dgn-gda:DGNefae2c6c5f3b6933388e91c4648b6051
sio:SIO_000628
miriam-gene:3673
,
lld:C0004943
;
a
sio:SIO_001122
.
}
dgn-np:NP55774.RATFbLZ0l8QSBvAP7oLxPi_bJYF667ZE5Io7gJaF6q2ug130_provenance
{
dgn-np:NP55774.RATFbLZ0l8QSBvAP7oLxPi_bJYF667ZE5Io7gJaF6q2ug130_assertion
dcterms:description
"[Our data indicate hat patients with BD are affected by the glycoprotein Ia gene 807TT genotypes and carrying 807T allele. The risk of thrombosis is significantly higher in patients who have 807TT and 807CT genotypes than in patients who have 807CC genotype.]. 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:12412731
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP55774.RATFbLZ0l8QSBvAP7oLxPi_bJYF667ZE5Io7gJaF6q2ug130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:26+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" .
}