@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk
> .
@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:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_head
{
this:
np:hasAssertion
dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_assertion
;
np:hasProvenance
dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_provenance
;
np:hasPublicationInfo
dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_assertion
a
np:Assertion
.
dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_provenance
a
np:Provenance
.
dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNf2ddf1297f24aabe2d1e4113811ba4ce
sio:SIO_000628
miriam-gene:324
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_provenance
{
dgn-np:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_assertion
dcterms:description
"[Because UEC and CRC share other molecular genetic alterations and histologic features and previous studies of UEC have not reported an analysis of the APC gene, we chose to further elucidate the role of the Wnt pathway in UEC.]. 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:11048799
;
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:NP171913.RAVc6bbPDL8xfWwg4-OjnO4pH8v1jioxZfZHLF0_lRQfk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:33+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" .
}