@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP309006.RAL6agLW-O24_-MCFnCgXGc2h5AnhY86bD0QxAQJ-_HZ0
> .
@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:NP309006.RAL6agLW-O24_-MCFnCgXGc2h5AnhY86bD0QxAQJ-_HZ0130_head
{
this:
np:hasAssertion
dgn-np:NP309006.RAL6agLW-O24_-MCFnCgXGc2h5AnhY86bD0QxAQJ-_HZ0130_assertion
;
np:hasProvenance
dgn-np:NP309006.RAL6agLW-O24_-MCFnCgXGc2h5AnhY86bD0QxAQJ-_HZ0130_provenance
;
np:hasPublicationInfo
dgn-np:NP309006.RAL6agLW-O24_-MCFnCgXGc2h5AnhY86bD0QxAQJ-_HZ0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP309006.RAL6agLW-O24_-MCFnCgXGc2h5AnhY86bD0QxAQJ-_HZ0130_assertion
a
np:Assertion
.
dgn-np:NP309006.RAL6agLW-O24_-MCFnCgXGc2h5AnhY86bD0QxAQJ-_HZ0130_provenance
a
np:Provenance
.
dgn-np:NP309006.RAL6agLW-O24_-MCFnCgXGc2h5AnhY86bD0QxAQJ-_HZ0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP309006.RAL6agLW-O24_-MCFnCgXGc2h5AnhY86bD0QxAQJ-_HZ0130_assertion
{
miriam-gene:540
a
ncit:C16612
.
lld:C0019202
a
ncit:C7057
.
dgn-gda:DGN8e7c5ea1f526cec371a27159746594f5
sio:SIO_000628
miriam-gene:540
,
lld:C0019202
;
a
sio:SIO_001121
.
}
dgn-np:NP309006.RAL6agLW-O24_-MCFnCgXGc2h5AnhY86bD0QxAQJ-_HZ0130_provenance
{
dgn-np:NP309006.RAL6agLW-O24_-MCFnCgXGc2h5AnhY86bD0QxAQJ-_HZ0130_assertion
dcterms:description
"[In this study, we report the further results of an ongoing project on the delineation of the spectrum of mutations on the ATP7B gene in Wilson disease (WD) patients of Greek origin.]. 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:11216666
;
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:NP309006.RAL6agLW-O24_-MCFnCgXGc2h5AnhY86bD0QxAQJ-_HZ0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:05+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" .
}