@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1331926.RAcIVsTKDhxBuG2pWrs1re7HnVpwuMzK9x9HuLO7qtl5U
> .
@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:NP1331926.RAcIVsTKDhxBuG2pWrs1re7HnVpwuMzK9x9HuLO7qtl5U130_head
{
this:
np:hasAssertion
dgn-np:NP1331926.RAcIVsTKDhxBuG2pWrs1re7HnVpwuMzK9x9HuLO7qtl5U130_assertion
;
np:hasProvenance
dgn-np:NP1331926.RAcIVsTKDhxBuG2pWrs1re7HnVpwuMzK9x9HuLO7qtl5U130_provenance
;
np:hasPublicationInfo
dgn-np:NP1331926.RAcIVsTKDhxBuG2pWrs1re7HnVpwuMzK9x9HuLO7qtl5U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1331926.RAcIVsTKDhxBuG2pWrs1re7HnVpwuMzK9x9HuLO7qtl5U130_assertion
a
np:Assertion
.
dgn-np:NP1331926.RAcIVsTKDhxBuG2pWrs1re7HnVpwuMzK9x9HuLO7qtl5U130_provenance
a
np:Provenance
.
dgn-np:NP1331926.RAcIVsTKDhxBuG2pWrs1re7HnVpwuMzK9x9HuLO7qtl5U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1331926.RAcIVsTKDhxBuG2pWrs1re7HnVpwuMzK9x9HuLO7qtl5U130_assertion
{
miriam-gene:540
a
ncit:C16612
.
lld:C0019202
a
ncit:C7057
.
dgn-gda:DGN852d40e9d7a3e96ad9549694b80f2dcd
sio:SIO_000628
miriam-gene:540
,
lld:C0019202
;
a
sio:SIO_001121
.
}
dgn-np:NP1331926.RAcIVsTKDhxBuG2pWrs1re7HnVpwuMzK9x9HuLO7qtl5U130_provenance
{
dgn-np:NP1331926.RAcIVsTKDhxBuG2pWrs1re7HnVpwuMzK9x9HuLO7qtl5U130_assertion
dcterms:description
"[Recently, however, two human diseases that disrupt copper transport, Menkes disease and Wilson disease, were found to be caused by mutations in two closely related genes, MNK and WND, which encode proteins belonging to the P-type ATPase family of cation transporters.]. 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:8091505
;
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:NP1331926.RAcIVsTKDhxBuG2pWrs1re7HnVpwuMzK9x9HuLO7qtl5U130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:50+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" .
}