@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP302741.RAFVch7ICzVXhwJXYKtKXNz3Lq_M4dye1xtGi-vzG1syA
> .
@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:NP302741.RAFVch7ICzVXhwJXYKtKXNz3Lq_M4dye1xtGi-vzG1syA130_head
{
this:
np:hasAssertion
dgn-np:NP302741.RAFVch7ICzVXhwJXYKtKXNz3Lq_M4dye1xtGi-vzG1syA130_assertion
;
np:hasProvenance
dgn-np:NP302741.RAFVch7ICzVXhwJXYKtKXNz3Lq_M4dye1xtGi-vzG1syA130_provenance
;
np:hasPublicationInfo
dgn-np:NP302741.RAFVch7ICzVXhwJXYKtKXNz3Lq_M4dye1xtGi-vzG1syA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP302741.RAFVch7ICzVXhwJXYKtKXNz3Lq_M4dye1xtGi-vzG1syA130_assertion
a
np:Assertion
.
dgn-np:NP302741.RAFVch7ICzVXhwJXYKtKXNz3Lq_M4dye1xtGi-vzG1syA130_provenance
a
np:Provenance
.
dgn-np:NP302741.RAFVch7ICzVXhwJXYKtKXNz3Lq_M4dye1xtGi-vzG1syA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP302741.RAFVch7ICzVXhwJXYKtKXNz3Lq_M4dye1xtGi-vzG1syA130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C2584409
a
ncit:C7057
.
dgn-gda:DGN43505a40fef9ef6f65ed2e2e866a524a
sio:SIO_000628
miriam-gene:2153
,
lld:C2584409
;
a
sio:SIO_001122
.
}
dgn-np:NP302741.RAFVch7ICzVXhwJXYKtKXNz3Lq_M4dye1xtGi-vzG1syA130_provenance
{
dgn-np:NP302741.RAFVch7ICzVXhwJXYKtKXNz3Lq_M4dye1xtGi-vzG1syA130_assertion
dcterms:description
"[The prothrombin G20210A mutation and factor V Leiden have been found to be associated with an increased risk of venous thrombosis, but the reported prevalences of the prothrombin gene variant both in the normal population and in patients with deep venous thrombosis (DVT) vary greatly in the literature.]. 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:11114134
;
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:NP302741.RAFVch7ICzVXhwJXYKtKXNz3Lq_M4dye1xtGi-vzG1syA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:02+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" .
}