@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP295088.RAUxMl6uaJJLDPDszk8akpBGFJYiOMNG3c7m-PDX0i_vk
> .
@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:NP295088.RAUxMl6uaJJLDPDszk8akpBGFJYiOMNG3c7m-PDX0i_vk130_head
{
this:
np:hasAssertion
dgn-np:NP295088.RAUxMl6uaJJLDPDszk8akpBGFJYiOMNG3c7m-PDX0i_vk130_assertion
;
np:hasProvenance
dgn-np:NP295088.RAUxMl6uaJJLDPDszk8akpBGFJYiOMNG3c7m-PDX0i_vk130_provenance
;
np:hasPublicationInfo
dgn-np:NP295088.RAUxMl6uaJJLDPDszk8akpBGFJYiOMNG3c7m-PDX0i_vk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295088.RAUxMl6uaJJLDPDszk8akpBGFJYiOMNG3c7m-PDX0i_vk130_assertion
a
np:Assertion
.
dgn-np:NP295088.RAUxMl6uaJJLDPDszk8akpBGFJYiOMNG3c7m-PDX0i_vk130_provenance
a
np:Provenance
.
dgn-np:NP295088.RAUxMl6uaJJLDPDszk8akpBGFJYiOMNG3c7m-PDX0i_vk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP295088.RAUxMl6uaJJLDPDszk8akpBGFJYiOMNG3c7m-PDX0i_vk130_assertion
{
miriam-gene:3479
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGNe682610c8eba8d4fc48c4883994c5027
sio:SIO_000628
miriam-gene:3479
,
lld:C0027051
;
a
sio:SIO_001121
.
}
dgn-np:NP295088.RAUxMl6uaJJLDPDszk8akpBGFJYiOMNG3c7m-PDX0i_vk130_provenance
{
dgn-np:NP295088.RAUxMl6uaJJLDPDszk8akpBGFJYiOMNG3c7m-PDX0i_vk130_assertion
dcterms:description
"[The aim of the present study was to investigate the relationship between the human IGF1 gene and myocardial infarction (MI) in the Japanese population via the use of single nucleotide polymorphisms (SNPs).]. 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:21039458
;
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:NP295088.RAUxMl6uaJJLDPDszk8akpBGFJYiOMNG3c7m-PDX0i_vk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}