@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP303337.RA4xnu_NoolO3nZIJ9mCJN9Ut1WwXpk0w_75cvjr6S8Dw
> .
@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:NP303337.RA4xnu_NoolO3nZIJ9mCJN9Ut1WwXpk0w_75cvjr6S8Dw130_head
{
this:
np:hasAssertion
dgn-np:NP303337.RA4xnu_NoolO3nZIJ9mCJN9Ut1WwXpk0w_75cvjr6S8Dw130_assertion
;
np:hasProvenance
dgn-np:NP303337.RA4xnu_NoolO3nZIJ9mCJN9Ut1WwXpk0w_75cvjr6S8Dw130_provenance
;
np:hasPublicationInfo
dgn-np:NP303337.RA4xnu_NoolO3nZIJ9mCJN9Ut1WwXpk0w_75cvjr6S8Dw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP303337.RA4xnu_NoolO3nZIJ9mCJN9Ut1WwXpk0w_75cvjr6S8Dw130_assertion
a
np:Assertion
.
dgn-np:NP303337.RA4xnu_NoolO3nZIJ9mCJN9Ut1WwXpk0w_75cvjr6S8Dw130_provenance
a
np:Provenance
.
dgn-np:NP303337.RA4xnu_NoolO3nZIJ9mCJN9Ut1WwXpk0w_75cvjr6S8Dw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP303337.RA4xnu_NoolO3nZIJ9mCJN9Ut1WwXpk0w_75cvjr6S8Dw130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C3272363
a
ncit:C7057
.
dgn-gda:DGN916b0b9e33c177f09734b1b10e3079eb
sio:SIO_000628
miriam-gene:2147
,
lld:C3272363
;
a
sio:SIO_001121
.
}
dgn-np:NP303337.RA4xnu_NoolO3nZIJ9mCJN9Ut1WwXpk0w_75cvjr6S8Dw130_provenance
{
dgn-np:NP303337.RA4xnu_NoolO3nZIJ9mCJN9Ut1WwXpk0w_75cvjr6S8Dw130_assertion
dcterms:description
"[In conclusion, our results indicate that FV Leiden mutation, prothrombin G20210A genotype, and homozygosity for the C677T mutation in the MTHFR gene are not associated with an increased risk for ischemic stroke in young adults.]. 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:11697722
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP303337.RA4xnu_NoolO3nZIJ9mCJN9Ut1WwXpk0w_75cvjr6S8Dw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:54+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" .
}