@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP494859.RATnzkIWNNzHXacBwfFcNlDJubGSexAcqEwTG03mHGiV0
> .
@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:NP494859.RATnzkIWNNzHXacBwfFcNlDJubGSexAcqEwTG03mHGiV0130_head
{
this:
np:hasAssertion
dgn-np:NP494859.RATnzkIWNNzHXacBwfFcNlDJubGSexAcqEwTG03mHGiV0130_assertion
;
np:hasProvenance
dgn-np:NP494859.RATnzkIWNNzHXacBwfFcNlDJubGSexAcqEwTG03mHGiV0130_provenance
;
np:hasPublicationInfo
dgn-np:NP494859.RATnzkIWNNzHXacBwfFcNlDJubGSexAcqEwTG03mHGiV0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP494859.RATnzkIWNNzHXacBwfFcNlDJubGSexAcqEwTG03mHGiV0130_assertion
a
np:Assertion
.
dgn-np:NP494859.RATnzkIWNNzHXacBwfFcNlDJubGSexAcqEwTG03mHGiV0130_provenance
a
np:Provenance
.
dgn-np:NP494859.RATnzkIWNNzHXacBwfFcNlDJubGSexAcqEwTG03mHGiV0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP494859.RATnzkIWNNzHXacBwfFcNlDJubGSexAcqEwTG03mHGiV0130_assertion
{
miriam-gene:100
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN8634e6b1221f6fb4d9563830685b1e6a
sio:SIO_000628
miriam-gene:100
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP494859.RATnzkIWNNzHXacBwfFcNlDJubGSexAcqEwTG03mHGiV0130_provenance
{
dgn-np:NP494859.RATnzkIWNNzHXacBwfFcNlDJubGSexAcqEwTG03mHGiV0130_assertion
dcterms:description
"[The fact that the association of ACP1 with CAD is evident only in diabetic subjects, whereas the association of ADA1 with CAD is evident only in nondiabetic subjects suggests an heterogeneity in the pathogenetic mechanisms leading to 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:20581655
;
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:NP494859.RATnzkIWNNzHXacBwfFcNlDJubGSexAcqEwTG03mHGiV0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:55+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" .
}