@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP938394.RAD2Rx4e8a9dB-aVYzSrq8GgMFLCaU6V-p8z49Z0JHfOc
> .
@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:NP938394.RAD2Rx4e8a9dB-aVYzSrq8GgMFLCaU6V-p8z49Z0JHfOc130_head
{
this:
np:hasAssertion
dgn-np:NP938394.RAD2Rx4e8a9dB-aVYzSrq8GgMFLCaU6V-p8z49Z0JHfOc130_assertion
;
np:hasProvenance
dgn-np:NP938394.RAD2Rx4e8a9dB-aVYzSrq8GgMFLCaU6V-p8z49Z0JHfOc130_provenance
;
np:hasPublicationInfo
dgn-np:NP938394.RAD2Rx4e8a9dB-aVYzSrq8GgMFLCaU6V-p8z49Z0JHfOc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP938394.RAD2Rx4e8a9dB-aVYzSrq8GgMFLCaU6V-p8z49Z0JHfOc130_assertion
a
np:Assertion
.
dgn-np:NP938394.RAD2Rx4e8a9dB-aVYzSrq8GgMFLCaU6V-p8z49Z0JHfOc130_provenance
a
np:Provenance
.
dgn-np:NP938394.RAD2Rx4e8a9dB-aVYzSrq8GgMFLCaU6V-p8z49Z0JHfOc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP938394.RAD2Rx4e8a9dB-aVYzSrq8GgMFLCaU6V-p8z49Z0JHfOc130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0699790
a
ncit:C7057
.
dgn-gda:DGN7a90b1955bc53c5cbb7d64a6ac656721
sio:SIO_000628
miriam-gene:348
,
lld:C0699790
;
a
sio:SIO_001121
.
}
dgn-np:NP938394.RAD2Rx4e8a9dB-aVYzSrq8GgMFLCaU6V-p8z49Z0JHfOc130_provenance
{
dgn-np:NP938394.RAD2Rx4e8a9dB-aVYzSrq8GgMFLCaU6V-p8z49Z0JHfOc130_assertion
dcterms:description
"[These findings suggest those apoE genotypes that do not include the e3 allele, the same genotypes that are associated with increased risk of coronary heart disease, may influence development of colon cancer among those who are older at diagnosis.]. 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:15817610
;
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:NP938394.RAD2Rx4e8a9dB-aVYzSrq8GgMFLCaU6V-p8z49Z0JHfOc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}