@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP448661.RAlK5QNxjfZFYfOG3mnGm15UHB4nWrYRr_mQB1XDXjcDM
> .
@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:NP448661.RAlK5QNxjfZFYfOG3mnGm15UHB4nWrYRr_mQB1XDXjcDM130_head
{
this:
np:hasAssertion
dgn-np:NP448661.RAlK5QNxjfZFYfOG3mnGm15UHB4nWrYRr_mQB1XDXjcDM130_assertion
;
np:hasProvenance
dgn-np:NP448661.RAlK5QNxjfZFYfOG3mnGm15UHB4nWrYRr_mQB1XDXjcDM130_provenance
;
np:hasPublicationInfo
dgn-np:NP448661.RAlK5QNxjfZFYfOG3mnGm15UHB4nWrYRr_mQB1XDXjcDM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP448661.RAlK5QNxjfZFYfOG3mnGm15UHB4nWrYRr_mQB1XDXjcDM130_assertion
a
np:Assertion
.
dgn-np:NP448661.RAlK5QNxjfZFYfOG3mnGm15UHB4nWrYRr_mQB1XDXjcDM130_provenance
a
np:Provenance
.
dgn-np:NP448661.RAlK5QNxjfZFYfOG3mnGm15UHB4nWrYRr_mQB1XDXjcDM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP448661.RAlK5QNxjfZFYfOG3mnGm15UHB4nWrYRr_mQB1XDXjcDM130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0026650
a
ncit:C7057
.
dgn-gda:DGN655b3731c4bdf4af84e7628d5e17ecfb
sio:SIO_000628
miriam-gene:3077
,
lld:C0026650
;
a
sio:SIO_001121
.
}
dgn-np:NP448661.RAlK5QNxjfZFYfOG3mnGm15UHB4nWrYRr_mQB1XDXjcDM130_provenance
{
dgn-np:NP448661.RAlK5QNxjfZFYfOG3mnGm15UHB4nWrYRr_mQB1XDXjcDM130_assertion
dcterms:description
"[Consistent with this, polymorphisms in the HFE gene, associated with the iron overload disorder hemochromatosis, show stronger associations with the movement disorder amyotrophic lateral sclerosis (motor neuron disease) than with cognitive impairment.]. 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:20345752
;
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:NP448661.RAlK5QNxjfZFYfOG3mnGm15UHB4nWrYRr_mQB1XDXjcDM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:27+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" .
}