@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP368877.RAp4D8JfKWxxgEIOgAk9NiyM5fb4xgOzjEsRAawddzdSg
> .
@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:NP368877.RAp4D8JfKWxxgEIOgAk9NiyM5fb4xgOzjEsRAawddzdSg130_head
{
this:
np:hasAssertion
dgn-np:NP368877.RAp4D8JfKWxxgEIOgAk9NiyM5fb4xgOzjEsRAawddzdSg130_assertion
;
np:hasProvenance
dgn-np:NP368877.RAp4D8JfKWxxgEIOgAk9NiyM5fb4xgOzjEsRAawddzdSg130_provenance
;
np:hasPublicationInfo
dgn-np:NP368877.RAp4D8JfKWxxgEIOgAk9NiyM5fb4xgOzjEsRAawddzdSg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP368877.RAp4D8JfKWxxgEIOgAk9NiyM5fb4xgOzjEsRAawddzdSg130_assertion
a
np:Assertion
.
dgn-np:NP368877.RAp4D8JfKWxxgEIOgAk9NiyM5fb4xgOzjEsRAawddzdSg130_provenance
a
np:Provenance
.
dgn-np:NP368877.RAp4D8JfKWxxgEIOgAk9NiyM5fb4xgOzjEsRAawddzdSg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP368877.RAp4D8JfKWxxgEIOgAk9NiyM5fb4xgOzjEsRAawddzdSg130_assertion
{
miriam-gene:6521
a
ncit:C16612
.
lld:C0019202
a
ncit:C7057
.
dgn-gda:DGN981e41faaefb9c78802a6b653b2c86b2
sio:SIO_000628
miriam-gene:6521
,
lld:C0019202
;
a
sio:SIO_001121
.
}
dgn-np:NP368877.RAp4D8JfKWxxgEIOgAk9NiyM5fb4xgOzjEsRAawddzdSg130_provenance
{
dgn-np:NP368877.RAp4D8JfKWxxgEIOgAk9NiyM5fb4xgOzjEsRAawddzdSg130_assertion
dcterms:description
"[The results produced in this study strongly suggest that DNA mutations residing in the consensus sequence of WD gene splice sites result in the WD phenotype by interfering with the production of the normal WD protein.]. 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:12325021
;
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:NP368877.RAp4D8JfKWxxgEIOgAk9NiyM5fb4xgOzjEsRAawddzdSg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:32+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" .
}