@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP747468.RA7dVW_Y9SSqEW3gD5aiZeSRVEhZ9Y44rfKgN_wNXh56g
> .
@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:NP747468.RA7dVW_Y9SSqEW3gD5aiZeSRVEhZ9Y44rfKgN_wNXh56g130_head
{
this:
np:hasAssertion
dgn-np:NP747468.RA7dVW_Y9SSqEW3gD5aiZeSRVEhZ9Y44rfKgN_wNXh56g130_assertion
;
np:hasProvenance
dgn-np:NP747468.RA7dVW_Y9SSqEW3gD5aiZeSRVEhZ9Y44rfKgN_wNXh56g130_provenance
;
np:hasPublicationInfo
dgn-np:NP747468.RA7dVW_Y9SSqEW3gD5aiZeSRVEhZ9Y44rfKgN_wNXh56g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP747468.RA7dVW_Y9SSqEW3gD5aiZeSRVEhZ9Y44rfKgN_wNXh56g130_assertion
a
np:Assertion
.
dgn-np:NP747468.RA7dVW_Y9SSqEW3gD5aiZeSRVEhZ9Y44rfKgN_wNXh56g130_provenance
a
np:Provenance
.
dgn-np:NP747468.RA7dVW_Y9SSqEW3gD5aiZeSRVEhZ9Y44rfKgN_wNXh56g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP747468.RA7dVW_Y9SSqEW3gD5aiZeSRVEhZ9Y44rfKgN_wNXh56g130_assertion
{
miriam-gene:10218
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGNa3a51d1ef1f09bef224a6ad2bc8422d9
sio:SIO_000628
miriam-gene:10218
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP747468.RA7dVW_Y9SSqEW3gD5aiZeSRVEhZ9Y44rfKgN_wNXh56g130_provenance
{
dgn-np:NP747468.RA7dVW_Y9SSqEW3gD5aiZeSRVEhZ9Y44rfKgN_wNXh56g130_assertion
dcterms:description
"[Of these, five loci showed highest methylation levels in HCC and lowest in control tissue (LOC55908, CELSR1, CRMP1, GNRH2, ALOX12 and ANGPTL7), whereas two loci showed the opposite direction of change (SPRR3 and TNFSF15).]. 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:21500188
;
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:NP747468.RA7dVW_Y9SSqEW3gD5aiZeSRVEhZ9Y44rfKgN_wNXh56g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:33+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" .
}