@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_head
{
this:
np:hasAssertion
dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_assertion
;
np:hasProvenance
dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_provenance
;
np:hasPublicationInfo
dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_assertion
a
np:Assertion
.
dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_provenance
a
np:Provenance
.
dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_assertion
{
miriam-gene:54894
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN30f62cc6bc74fdc4e435802e1a5bb08f
sio:SIO_000628
miriam-gene:54894
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_provenance
{
dgn-np:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_assertion
dcterms:description
"[A new study suggests that RNF43 is one of the most commonly mutated genes in endometrial and colorectal cancers and may help identify patients who could potentially benefit from drugs that target the Wnt signaling pathway.]. 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:25583782
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1255062.RAH1beAoJX4Lc83pWl5Qi65dEWFQvx2nySPC5MnjltbCA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:15+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}