@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP295922.RADi_Otoxb0_iqW3C-SVXke-j40qeDVjX1XH0zOWM3S2o
> .
@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:NP295922.RADi_Otoxb0_iqW3C-SVXke-j40qeDVjX1XH0zOWM3S2o130_head
{
this:
np:hasAssertion
dgn-np:NP295922.RADi_Otoxb0_iqW3C-SVXke-j40qeDVjX1XH0zOWM3S2o130_assertion
;
np:hasProvenance
dgn-np:NP295922.RADi_Otoxb0_iqW3C-SVXke-j40qeDVjX1XH0zOWM3S2o130_provenance
;
np:hasPublicationInfo
dgn-np:NP295922.RADi_Otoxb0_iqW3C-SVXke-j40qeDVjX1XH0zOWM3S2o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295922.RADi_Otoxb0_iqW3C-SVXke-j40qeDVjX1XH0zOWM3S2o130_assertion
a
np:Assertion
.
dgn-np:NP295922.RADi_Otoxb0_iqW3C-SVXke-j40qeDVjX1XH0zOWM3S2o130_provenance
a
np:Provenance
.
dgn-np:NP295922.RADi_Otoxb0_iqW3C-SVXke-j40qeDVjX1XH0zOWM3S2o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP295922.RADi_Otoxb0_iqW3C-SVXke-j40qeDVjX1XH0zOWM3S2o130_assertion
{
miriam-gene:5554
a
ncit:C16612
.
lld:C0398623
a
ncit:C7057
.
dgn-gda:DGNe759cf849283c5af89011e0c38f661dc
sio:SIO_000628
miriam-gene:5554
,
lld:C0398623
;
a
sio:SIO_001121
.
}
dgn-np:NP295922.RADi_Otoxb0_iqW3C-SVXke-j40qeDVjX1XH0zOWM3S2o130_provenance
{
dgn-np:NP295922.RADi_Otoxb0_iqW3C-SVXke-j40qeDVjX1XH0zOWM3S2o130_assertion
dcterms:description
"[Abnormalities in haemostasis that are associated with clinical thrombophilia include heritable defects, such as mutations in the genes encoding the natural anticoagulants antithrombin, protein C, and protein S, or clotting factors prothrombin and factor V, and acquired defects, such as antiphospholipids.]. 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:11002758
;
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:NP295922.RADi_Otoxb0_iqW3C-SVXke-j40qeDVjX1XH0zOWM3S2o130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:00+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" .
}