@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP725260.RAwL94Hx5qYJgwDjMVoDRIf5fV5hbqJIlpUW_so0N5-lA
> .
@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:NP725260.RAwL94Hx5qYJgwDjMVoDRIf5fV5hbqJIlpUW_so0N5-lA130_head
{
this:
np:hasAssertion
dgn-np:NP725260.RAwL94Hx5qYJgwDjMVoDRIf5fV5hbqJIlpUW_so0N5-lA130_assertion
;
np:hasProvenance
dgn-np:NP725260.RAwL94Hx5qYJgwDjMVoDRIf5fV5hbqJIlpUW_so0N5-lA130_provenance
;
np:hasPublicationInfo
dgn-np:NP725260.RAwL94Hx5qYJgwDjMVoDRIf5fV5hbqJIlpUW_so0N5-lA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP725260.RAwL94Hx5qYJgwDjMVoDRIf5fV5hbqJIlpUW_so0N5-lA130_assertion
a
np:Assertion
.
dgn-np:NP725260.RAwL94Hx5qYJgwDjMVoDRIf5fV5hbqJIlpUW_so0N5-lA130_provenance
a
np:Provenance
.
dgn-np:NP725260.RAwL94Hx5qYJgwDjMVoDRIf5fV5hbqJIlpUW_so0N5-lA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP725260.RAwL94Hx5qYJgwDjMVoDRIf5fV5hbqJIlpUW_so0N5-lA130_assertion
{
miriam-gene:8398
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNe0a7e5859ff0604894c0ca38a881386e
sio:SIO_000628
miriam-gene:8398
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP725260.RAwL94Hx5qYJgwDjMVoDRIf5fV5hbqJIlpUW_so0N5-lA130_provenance
{
dgn-np:NP725260.RAwL94Hx5qYJgwDjMVoDRIf5fV5hbqJIlpUW_so0N5-lA130_assertion
dcterms:description
"[Whereas no difference in the distribution of allele and genotype frequencies between controls and survivors of MI could be detected, the PlA2 allele is associated with CHD in low risk patients.]. 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:9716139
;
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:NP725260.RAwL94Hx5qYJgwDjMVoDRIf5fV5hbqJIlpUW_so0N5-lA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}