@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP183465.RAz9Q0Yf2V_T2shqVJl8N8mO2J4dRVTYLy_DEBYOTITJE
> .
@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:NP183465.RAz9Q0Yf2V_T2shqVJl8N8mO2J4dRVTYLy_DEBYOTITJE130_head
{
this:
np:hasAssertion
dgn-np:NP183465.RAz9Q0Yf2V_T2shqVJl8N8mO2J4dRVTYLy_DEBYOTITJE130_assertion
;
np:hasProvenance
dgn-np:NP183465.RAz9Q0Yf2V_T2shqVJl8N8mO2J4dRVTYLy_DEBYOTITJE130_provenance
;
np:hasPublicationInfo
dgn-np:NP183465.RAz9Q0Yf2V_T2shqVJl8N8mO2J4dRVTYLy_DEBYOTITJE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP183465.RAz9Q0Yf2V_T2shqVJl8N8mO2J4dRVTYLy_DEBYOTITJE130_assertion
a
np:Assertion
.
dgn-np:NP183465.RAz9Q0Yf2V_T2shqVJl8N8mO2J4dRVTYLy_DEBYOTITJE130_provenance
a
np:Provenance
.
dgn-np:NP183465.RAz9Q0Yf2V_T2shqVJl8N8mO2J4dRVTYLy_DEBYOTITJE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP183465.RAz9Q0Yf2V_T2shqVJl8N8mO2J4dRVTYLy_DEBYOTITJE130_assertion
{
miriam-gene:538
a
ncit:C16612
.
lld:C0022716
a
ncit:C7057
.
dgn-gda:DGN2c12c66ed1366c181ab93af5c1d623b2
sio:SIO_000628
miriam-gene:538
,
lld:C0022716
;
a
sio:SIO_001121
.
}
dgn-np:NP183465.RAz9Q0Yf2V_T2shqVJl8N8mO2J4dRVTYLy_DEBYOTITJE130_provenance
{
dgn-np:NP183465.RAz9Q0Yf2V_T2shqVJl8N8mO2J4dRVTYLy_DEBYOTITJE130_assertion
dcterms:description
"[Adequate supplies of copper are particularly important in developing animals, and in humans this is illustrated by mutations of ATP7A that cause the copper deficiency condition Menkes disease, which is fatal in early childhood.]. 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:12730448
;
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:NP183465.RAz9Q0Yf2V_T2shqVJl8N8mO2J4dRVTYLy_DEBYOTITJE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:39+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" .
}