@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP53007.RAlfCKkH3DzJQ6AzlFI22IfAhYrNHsb-DsIr4AW0SERGc
> .
@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/v3.0.0/void/
> .
dgn-np:NP53007.RAlfCKkH3DzJQ6AzlFI22IfAhYrNHsb-DsIr4AW0SERGc130_head
{
this:
np:hasAssertion
dgn-np:NP53007.RAlfCKkH3DzJQ6AzlFI22IfAhYrNHsb-DsIr4AW0SERGc130_assertion
;
np:hasProvenance
dgn-np:NP53007.RAlfCKkH3DzJQ6AzlFI22IfAhYrNHsb-DsIr4AW0SERGc130_provenance
;
np:hasPublicationInfo
dgn-np:NP53007.RAlfCKkH3DzJQ6AzlFI22IfAhYrNHsb-DsIr4AW0SERGc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53007.RAlfCKkH3DzJQ6AzlFI22IfAhYrNHsb-DsIr4AW0SERGc130_assertion
a
np:Assertion
.
dgn-np:NP53007.RAlfCKkH3DzJQ6AzlFI22IfAhYrNHsb-DsIr4AW0SERGc130_provenance
a
np:Provenance
.
dgn-np:NP53007.RAlfCKkH3DzJQ6AzlFI22IfAhYrNHsb-DsIr4AW0SERGc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53007.RAlfCKkH3DzJQ6AzlFI22IfAhYrNHsb-DsIr4AW0SERGc130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGNfc3b89d2567e3c02dfe7e71758698715
sio:SIO_000628
miriam-gene:2147
,
lld:C0027051
;
a
sio:SIO_001122
.
}
dgn-np:NP53007.RAlfCKkH3DzJQ6AzlFI22IfAhYrNHsb-DsIr4AW0SERGc130_provenance
{
dgn-np:NP53007.RAlfCKkH3DzJQ6AzlFI22IfAhYrNHsb-DsIr4AW0SERGc130_assertion
dcterms:description
"[In a large cohort of young AMI patients the gain-of-function variant F5 G1691A was associated with an increased risk of AMI. The findings on the variant F2 G20210A confirmed the previously reported results, but the association was statistically not signif]. 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:20626623
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP53007.RAlfCKkH3DzJQ6AzlFI22IfAhYrNHsb-DsIr4AW0SERGc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:09+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}