@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE
> .
@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:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_head
{
this:
np:hasAssertion
dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_assertion
;
np:hasProvenance
dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_provenance
;
np:hasPublicationInfo
dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_assertion
a
np:Assertion
.
dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_provenance
a
np:Provenance
.
dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN10df39742d3cd0b1a5548e5eb1289bd7
sio:SIO_000628
miriam-gene:3077
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_provenance
{
dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_assertion
dcterms:description
"[HFE participates in the regulation of iron metabolism, its mutations are primary cause of hereditary hemochromatosis and appear to be more frequent in neurodegenerative disorders such as Alzheimer's disease and amyotrophic lateral sclerosis.]. 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:18325820
;
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:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:17+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" .
}