@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q
> .
@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:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_head
{
this:
np:hasAssertion
dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_assertion
;
np:hasProvenance
dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_assertion
a
np:Assertion
.
dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_provenance
a
np:Provenance
.
dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_assertion
{
miriam-gene:1499
a
ncit:C16612
.
lld:C0029925
a
ncit:C7057
.
dgn-gda:DGNadb34b8cf48ccd1093737c5de90939aa
sio:SIO_000628
miriam-gene:1499
,
lld:C0029925
;
a
sio:SIO_001121
.
}
dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_provenance
{
dgn-np:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_assertion
dcterms:description
"[Mutations in the beta-catenin (CTNNB1) gene have been recently reported in a small percentage of UECs and in the endometrioid variant of ovarian carcinoma suggesting that the Wnt signal transduction pathway is involved in the development of female genital tract tumors with endometrioid morphology.]. 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:NP237258.RAOzO7Xdpm4OD3eSUH67hOR0sHUl01IGd5vGNTXourh9Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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" .
}