@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP634579.RAYH968Xb26vobTAVW1nQfQMDR61JQvrvjcfVW0f11aSo
> .
@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:NP634579.RAYH968Xb26vobTAVW1nQfQMDR61JQvrvjcfVW0f11aSo130_head
{
this:
np:hasAssertion
dgn-np:NP634579.RAYH968Xb26vobTAVW1nQfQMDR61JQvrvjcfVW0f11aSo130_assertion
;
np:hasProvenance
dgn-np:NP634579.RAYH968Xb26vobTAVW1nQfQMDR61JQvrvjcfVW0f11aSo130_provenance
;
np:hasPublicationInfo
dgn-np:NP634579.RAYH968Xb26vobTAVW1nQfQMDR61JQvrvjcfVW0f11aSo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP634579.RAYH968Xb26vobTAVW1nQfQMDR61JQvrvjcfVW0f11aSo130_assertion
a
np:Assertion
.
dgn-np:NP634579.RAYH968Xb26vobTAVW1nQfQMDR61JQvrvjcfVW0f11aSo130_provenance
a
np:Provenance
.
dgn-np:NP634579.RAYH968Xb26vobTAVW1nQfQMDR61JQvrvjcfVW0f11aSo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP634579.RAYH968Xb26vobTAVW1nQfQMDR61JQvrvjcfVW0f11aSo130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0206624
a
ncit:C7057
.
dgn-gda:DGN1afd39b8bee832493a11534d047f0b53
sio:SIO_000628
miriam-gene:1956
,
lld:C0206624
;
a
sio:SIO_001121
.
}
dgn-np:NP634579.RAYH968Xb26vobTAVW1nQfQMDR61JQvrvjcfVW0f11aSo130_provenance
{
dgn-np:NP634579.RAYH968Xb26vobTAVW1nQfQMDR61JQvrvjcfVW0f11aSo130_assertion
dcterms:description
"[We studied the activation status of the Wnt and Notch pathways and the differential expression of hepatocyte nuclear factor 4alpha, EGFR, and IGF2 genes, relevant to liver development and malignant transformation in histologic variants of hepatoblastoma.]. 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:19200579
;
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:NP634579.RAYH968Xb26vobTAVW1nQfQMDR61JQvrvjcfVW0f11aSo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:23+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" .
}