@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP802717.RANRS52ha6pywmJSevyjKCiCuzpQAllDU5bqlKNo67fxY
> .
@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:NP802717.RANRS52ha6pywmJSevyjKCiCuzpQAllDU5bqlKNo67fxY130_head
{
this:
np:hasAssertion
dgn-np:NP802717.RANRS52ha6pywmJSevyjKCiCuzpQAllDU5bqlKNo67fxY130_assertion
;
np:hasProvenance
dgn-np:NP802717.RANRS52ha6pywmJSevyjKCiCuzpQAllDU5bqlKNo67fxY130_provenance
;
np:hasPublicationInfo
dgn-np:NP802717.RANRS52ha6pywmJSevyjKCiCuzpQAllDU5bqlKNo67fxY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP802717.RANRS52ha6pywmJSevyjKCiCuzpQAllDU5bqlKNo67fxY130_assertion
a
np:Assertion
.
dgn-np:NP802717.RANRS52ha6pywmJSevyjKCiCuzpQAllDU5bqlKNo67fxY130_provenance
a
np:Provenance
.
dgn-np:NP802717.RANRS52ha6pywmJSevyjKCiCuzpQAllDU5bqlKNo67fxY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP802717.RANRS52ha6pywmJSevyjKCiCuzpQAllDU5bqlKNo67fxY130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0282193
a
ncit:C7057
.
dgn-gda:DGN42a56206df7cc72fd7d67dc6262ca99f
sio:SIO_000628
miriam-gene:3077
,
lld:C0282193
;
a
sio:SIO_001121
.
}
dgn-np:NP802717.RANRS52ha6pywmJSevyjKCiCuzpQAllDU5bqlKNo67fxY130_provenance
{
dgn-np:NP802717.RANRS52ha6pywmJSevyjKCiCuzpQAllDU5bqlKNo67fxY130_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-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:NP802717.RANRS52ha6pywmJSevyjKCiCuzpQAllDU5bqlKNo67fxY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:49+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" .
}