@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1224034.RAeJ2-_In_5Td9TuWBgU4wX7B987d8vBxJZv0NTncaRqM
> .
@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:NP1224034.RAeJ2-_In_5Td9TuWBgU4wX7B987d8vBxJZv0NTncaRqM130_head
{
this:
np:hasAssertion
dgn-np:NP1224034.RAeJ2-_In_5Td9TuWBgU4wX7B987d8vBxJZv0NTncaRqM130_assertion
;
np:hasProvenance
dgn-np:NP1224034.RAeJ2-_In_5Td9TuWBgU4wX7B987d8vBxJZv0NTncaRqM130_provenance
;
np:hasPublicationInfo
dgn-np:NP1224034.RAeJ2-_In_5Td9TuWBgU4wX7B987d8vBxJZv0NTncaRqM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1224034.RAeJ2-_In_5Td9TuWBgU4wX7B987d8vBxJZv0NTncaRqM130_assertion
a
np:Assertion
.
dgn-np:NP1224034.RAeJ2-_In_5Td9TuWBgU4wX7B987d8vBxJZv0NTncaRqM130_provenance
a
np:Provenance
.
dgn-np:NP1224034.RAeJ2-_In_5Td9TuWBgU4wX7B987d8vBxJZv0NTncaRqM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1224034.RAeJ2-_In_5Td9TuWBgU4wX7B987d8vBxJZv0NTncaRqM130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C1260403
a
ncit:C7057
.
dgn-gda:DGN26fae28cda6aa9b64a6bc78e0de647ff
sio:SIO_000628
miriam-gene:2153
,
lld:C1260403
;
a
sio:SIO_001121
.
}
dgn-np:NP1224034.RAeJ2-_In_5Td9TuWBgU4wX7B987d8vBxJZv0NTncaRqM130_provenance
{
dgn-np:NP1224034.RAeJ2-_In_5Td9TuWBgU4wX7B987d8vBxJZv0NTncaRqM130_assertion
dcterms:description
"[Despite higher frequency in patients compared to controls, there was no risk of association between prothrombin gene mutation and acute leukemia in adult Egyptians nor was there between combined genotypes of prothrombin gene mutation and factor V Leiden.]. 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:25260809
;
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:NP1224034.RAeJ2-_In_5Td9TuWBgU4wX7B987d8vBxJZv0NTncaRqM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:00+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" .
}