@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP940164.RAEvPxenXD3UrHX1iSd5rZZOswH5SHMaHBwjGOVKUet9k
> .
@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/v3.0.0/void/
> .
dgn-np:NP940164.RAEvPxenXD3UrHX1iSd5rZZOswH5SHMaHBwjGOVKUet9k130_head
{
this:
np:hasAssertion
dgn-np:NP940164.RAEvPxenXD3UrHX1iSd5rZZOswH5SHMaHBwjGOVKUet9k130_assertion
;
np:hasProvenance
dgn-np:NP940164.RAEvPxenXD3UrHX1iSd5rZZOswH5SHMaHBwjGOVKUet9k130_provenance
;
np:hasPublicationInfo
dgn-np:NP940164.RAEvPxenXD3UrHX1iSd5rZZOswH5SHMaHBwjGOVKUet9k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP940164.RAEvPxenXD3UrHX1iSd5rZZOswH5SHMaHBwjGOVKUet9k130_assertion
a
np:Assertion
.
dgn-np:NP940164.RAEvPxenXD3UrHX1iSd5rZZOswH5SHMaHBwjGOVKUet9k130_provenance
a
np:Provenance
.
dgn-np:NP940164.RAEvPxenXD3UrHX1iSd5rZZOswH5SHMaHBwjGOVKUet9k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP940164.RAEvPxenXD3UrHX1iSd5rZZOswH5SHMaHBwjGOVKUet9k130_assertion
{
miriam-gene:64840
a
ncit:C16612
.
lld:C0016395
a
ncit:C7057
.
dgn-gda:DGNb0896944e46c55990371f76be4975df6
sio:SIO_000628
miriam-gene:64840
,
lld:C0016395
;
a
sio:SIO_001121
.
}
dgn-np:NP940164.RAEvPxenXD3UrHX1iSd5rZZOswH5SHMaHBwjGOVKUet9k130_provenance
{
dgn-np:NP940164.RAEvPxenXD3UrHX1iSd5rZZOswH5SHMaHBwjGOVKUet9k130_assertion
dcterms:description
"[Since features of FDH overlap with those seen in mouse Wnt pathway mutants, FDH likely results from defective Wnt signaling but molecular mechanisms by which inactivation of PORCN affects Wnt signaling and manifestations of FDH remain to be elucidated.]. 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:22412863
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP940164.RAEvPxenXD3UrHX1iSd5rZZOswH5SHMaHBwjGOVKUet9k130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:14+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}