@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc
> .
@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:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_head
{
this:
np:hasAssertion
dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_assertion
;
np:hasProvenance
dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_provenance
;
np:hasPublicationInfo
dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_assertion
a
np:Assertion
.
dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_provenance
a
np:Provenance
.
dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_assertion
{
miriam-gene:1356
a
ncit:C16612
.
lld:C0152457
a
ncit:C7057
.
dgn-gda:DGNe914ef03f2bcf0d76b3f672e3de01a30
sio:SIO_000628
miriam-gene:1356
,
lld:C0152457
;
a
sio:SIO_001121
.
}
dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_provenance
{
dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_assertion
dcterms:description
"[Diagnosis is based on the combination of clinical features and findings such as increased urinary copper excretion, reduced levels of serum ceruloplasmin, high concentrations of copper in liver tissues and Kayser-Fleischer rings.]. 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:17382611
;
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:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+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" .
}