@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP242370.RABQwcJf-NhXAoDgzQeGNgKEm9wu5vBchMUuGKJw7hdws
> .
@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:NP242370.RABQwcJf-NhXAoDgzQeGNgKEm9wu5vBchMUuGKJw7hdws130_head
{
this:
np:hasAssertion
dgn-np:NP242370.RABQwcJf-NhXAoDgzQeGNgKEm9wu5vBchMUuGKJw7hdws130_assertion
;
np:hasProvenance
dgn-np:NP242370.RABQwcJf-NhXAoDgzQeGNgKEm9wu5vBchMUuGKJw7hdws130_provenance
;
np:hasPublicationInfo
dgn-np:NP242370.RABQwcJf-NhXAoDgzQeGNgKEm9wu5vBchMUuGKJw7hdws130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP242370.RABQwcJf-NhXAoDgzQeGNgKEm9wu5vBchMUuGKJw7hdws130_assertion
a
np:Assertion
.
dgn-np:NP242370.RABQwcJf-NhXAoDgzQeGNgKEm9wu5vBchMUuGKJw7hdws130_provenance
a
np:Provenance
.
dgn-np:NP242370.RABQwcJf-NhXAoDgzQeGNgKEm9wu5vBchMUuGKJw7hdws130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP242370.RABQwcJf-NhXAoDgzQeGNgKEm9wu5vBchMUuGKJw7hdws130_assertion
{
miriam-gene:100048912
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN3a3272edbc8c64ddf2ae9d95f62c4962
sio:SIO_000628
miriam-gene:100048912
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP242370.RABQwcJf-NhXAoDgzQeGNgKEm9wu5vBchMUuGKJw7hdws130_provenance
{
dgn-np:NP242370.RABQwcJf-NhXAoDgzQeGNgKEm9wu5vBchMUuGKJw7hdws130_assertion
dcterms:description
"[Elucidation of the interplay of ANRIL transcript variants and their involvement in increased susceptibility to the interactive diseases CHD and periodontitis promises new insight into the underlying shared pathogenic mechanisms of these complex common diseases.]. 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:19214202
;
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:NP242370.RABQwcJf-NhXAoDgzQeGNgKEm9wu5vBchMUuGKJw7hdws130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:15+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" .
}