@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14
> .
@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:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_head
{
this:
np:hasAssertion
dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_assertion
;
np:hasProvenance
dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_provenance
;
np:hasPublicationInfo
dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_assertion
a
np:Assertion
.
dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_provenance
a
np:Provenance
.
dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_assertion
{
miriam-gene:538
a
ncit:C16612
.
lld:C0268070
a
ncit:C7057
.
dgn-gda:DGNd0feb8a4c4c666469c13a8df53870a97
sio:SIO_000628
miriam-gene:538
,
lld:C0268070
;
a
sio:SIO_001121
.
}
dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_provenance
{
dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_assertion
dcterms:description
"[In more than 40 years since copper deficiency was delineated in pediatric subjects with Menkes disease, remarkable advances in our understanding of the clinical, biochemical, and molecular aspects of the human copper transporter ATP7A have emerged.]. 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:24735419
;
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:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:06+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" .
}