@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP903582.RAbvS3uqzIVDN3yqAphkm7-QsXjEoS_2pOuZ2dw73MDNE
> .
@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:NP903582.RAbvS3uqzIVDN3yqAphkm7-QsXjEoS_2pOuZ2dw73MDNE130_head
{
this:
np:hasAssertion
dgn-np:NP903582.RAbvS3uqzIVDN3yqAphkm7-QsXjEoS_2pOuZ2dw73MDNE130_assertion
;
np:hasProvenance
dgn-np:NP903582.RAbvS3uqzIVDN3yqAphkm7-QsXjEoS_2pOuZ2dw73MDNE130_provenance
;
np:hasPublicationInfo
dgn-np:NP903582.RAbvS3uqzIVDN3yqAphkm7-QsXjEoS_2pOuZ2dw73MDNE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP903582.RAbvS3uqzIVDN3yqAphkm7-QsXjEoS_2pOuZ2dw73MDNE130_assertion
a
np:Assertion
.
dgn-np:NP903582.RAbvS3uqzIVDN3yqAphkm7-QsXjEoS_2pOuZ2dw73MDNE130_provenance
a
np:Provenance
.
dgn-np:NP903582.RAbvS3uqzIVDN3yqAphkm7-QsXjEoS_2pOuZ2dw73MDNE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP903582.RAbvS3uqzIVDN3yqAphkm7-QsXjEoS_2pOuZ2dw73MDNE130_assertion
{
miriam-gene:1844
a
ncit:C16612
.
lld:C1458155
a
ncit:C7057
.
dgn-gda:DGN8d85c3cba83bd895abff1b67c218eee3
sio:SIO_000628
miriam-gene:1844
,
lld:C1458155
;
a
sio:SIO_001121
.
}
dgn-np:NP903582.RAbvS3uqzIVDN3yqAphkm7-QsXjEoS_2pOuZ2dw73MDNE130_provenance
{
dgn-np:NP903582.RAbvS3uqzIVDN3yqAphkm7-QsXjEoS_2pOuZ2dw73MDNE130_assertion
dcterms:description
"[Furthermore, by examining a panel of human breast tumor lines and primary tumors we observed that the human orthologs of ATP1B2, FOXJ1 and SMPD3 are aberrantly hypermethylated in the human disease whereas DUSP2 was not hypermethylated in primary breast tumors.]. 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:18836996
;
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:NP903582.RAbvS3uqzIVDN3yqAphkm7-QsXjEoS_2pOuZ2dw73MDNE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:15+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" .
}