@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP257089.RA3ias9e4FMMShyTGXhrutkoBxQ1DMW6WjiIhNWWSM0iY
> .
@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:NP257089.RA3ias9e4FMMShyTGXhrutkoBxQ1DMW6WjiIhNWWSM0iY130_head
{
this:
np:hasAssertion
dgn-np:NP257089.RA3ias9e4FMMShyTGXhrutkoBxQ1DMW6WjiIhNWWSM0iY130_assertion
;
np:hasProvenance
dgn-np:NP257089.RA3ias9e4FMMShyTGXhrutkoBxQ1DMW6WjiIhNWWSM0iY130_provenance
;
np:hasPublicationInfo
dgn-np:NP257089.RA3ias9e4FMMShyTGXhrutkoBxQ1DMW6WjiIhNWWSM0iY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP257089.RA3ias9e4FMMShyTGXhrutkoBxQ1DMW6WjiIhNWWSM0iY130_assertion
a
np:Assertion
.
dgn-np:NP257089.RA3ias9e4FMMShyTGXhrutkoBxQ1DMW6WjiIhNWWSM0iY130_provenance
a
np:Provenance
.
dgn-np:NP257089.RA3ias9e4FMMShyTGXhrutkoBxQ1DMW6WjiIhNWWSM0iY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP257089.RA3ias9e4FMMShyTGXhrutkoBxQ1DMW6WjiIhNWWSM0iY130_assertion
{
miriam-gene:538
a
ncit:C16612
.
lld:C0019202
a
ncit:C7057
.
dgn-gda:DGN4905b8952855cc41e72d82f2367936b9
sio:SIO_000628
miriam-gene:538
,
lld:C0019202
;
a
sio:SIO_001121
.
}
dgn-np:NP257089.RA3ias9e4FMMShyTGXhrutkoBxQ1DMW6WjiIhNWWSM0iY130_provenance
{
dgn-np:NP257089.RA3ias9e4FMMShyTGXhrutkoBxQ1DMW6WjiIhNWWSM0iY130_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-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:NP257089.RA3ias9e4FMMShyTGXhrutkoBxQ1DMW6WjiIhNWWSM0iY130_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" .
}