@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1063409.RA1kubj4pRa3mqP-4CQkJMRUlyanb-fxErninpWswwU_I
> .
@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/v4.0.0/void/
> .
dgn-np:NP1063409.RA1kubj4pRa3mqP-4CQkJMRUlyanb-fxErninpWswwU_I130_head
{
this:
np:hasAssertion
dgn-np:NP1063409.RA1kubj4pRa3mqP-4CQkJMRUlyanb-fxErninpWswwU_I130_assertion
;
np:hasProvenance
dgn-np:NP1063409.RA1kubj4pRa3mqP-4CQkJMRUlyanb-fxErninpWswwU_I130_provenance
;
np:hasPublicationInfo
dgn-np:NP1063409.RA1kubj4pRa3mqP-4CQkJMRUlyanb-fxErninpWswwU_I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1063409.RA1kubj4pRa3mqP-4CQkJMRUlyanb-fxErninpWswwU_I130_assertion
a
np:Assertion
.
dgn-np:NP1063409.RA1kubj4pRa3mqP-4CQkJMRUlyanb-fxErninpWswwU_I130_provenance
a
np:Provenance
.
dgn-np:NP1063409.RA1kubj4pRa3mqP-4CQkJMRUlyanb-fxErninpWswwU_I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1063409.RA1kubj4pRa3mqP-4CQkJMRUlyanb-fxErninpWswwU_I130_assertion
{
miriam-gene:124872
a
ncit:C16612
.
lld:C0018802
a
ncit:C7057
.
dgn-gda:DGN8dcb7844c757b53451b99366d802f4f2
sio:SIO_000628
miriam-gene:124872
,
lld:C0018802
;
a
sio:SIO_001121
.
}
dgn-np:NP1063409.RA1kubj4pRa3mqP-4CQkJMRUlyanb-fxErninpWswwU_I130_provenance
{
dgn-np:NP1063409.RA1kubj4pRa3mqP-4CQkJMRUlyanb-fxErninpWswwU_I130_assertion
dcterms:description
"[In addition, differences in the allelic and the genotypic frequencies of homozygous genotypes were found between the HF patients free from evidence of coronary significant lesions and patients with at least one hemodynamically significant coronary lesion, both HF and CAD.]. 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:23527722
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1063409.RA1kubj4pRa3mqP-4CQkJMRUlyanb-fxErninpWswwU_I130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:48+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: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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}