@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP627280.RAfs_0gUlDgxpGceICcb139GzPK9jyNssRwozdWDotYiU
> .
@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:NP627280.RAfs_0gUlDgxpGceICcb139GzPK9jyNssRwozdWDotYiU130_head
{
this:
np:hasAssertion
dgn-np:NP627280.RAfs_0gUlDgxpGceICcb139GzPK9jyNssRwozdWDotYiU130_assertion
;
np:hasProvenance
dgn-np:NP627280.RAfs_0gUlDgxpGceICcb139GzPK9jyNssRwozdWDotYiU130_provenance
;
np:hasPublicationInfo
dgn-np:NP627280.RAfs_0gUlDgxpGceICcb139GzPK9jyNssRwozdWDotYiU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP627280.RAfs_0gUlDgxpGceICcb139GzPK9jyNssRwozdWDotYiU130_assertion
a
np:Assertion
.
dgn-np:NP627280.RAfs_0gUlDgxpGceICcb139GzPK9jyNssRwozdWDotYiU130_provenance
a
np:Provenance
.
dgn-np:NP627280.RAfs_0gUlDgxpGceICcb139GzPK9jyNssRwozdWDotYiU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP627280.RAfs_0gUlDgxpGceICcb139GzPK9jyNssRwozdWDotYiU130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0155626
a
ncit:C7057
.
dgn-gda:DGN9abe8e66c29ac7701dce243aa5e4cd04
sio:SIO_000628
miriam-gene:2147
,
lld:C0155626
;
a
sio:SIO_001121
.
}
dgn-np:NP627280.RAfs_0gUlDgxpGceICcb139GzPK9jyNssRwozdWDotYiU130_provenance
{
dgn-np:NP627280.RAfs_0gUlDgxpGceICcb139GzPK9jyNssRwozdWDotYiU130_assertion
dcterms:description
"[In all the studies we examined, the polymorphism G20210A in the prothrombin gene was associated with an increased risk of acute myocardial infarction (AMI) in young people, especially when other risk factors were present.]. 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:15284679
;
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:NP627280.RAfs_0gUlDgxpGceICcb139GzPK9jyNssRwozdWDotYiU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:18+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" .
}