@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA
> .
@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:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_head
{
this:
np:hasAssertion
dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_assertion
;
np:hasProvenance
dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_provenance
;
np:hasPublicationInfo
dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_assertion
a
np:Assertion
.
dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_provenance
a
np:Provenance
.
dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0009088
a
ncit:C7057
.
dgn-gda:DGN73514d4955e56970443778c77e2dfb40
sio:SIO_000628
miriam-gene:3077
,
lld:C0009088
;
a
sio:SIO_001121
.
}
dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_provenance
{
dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_assertion
dcterms:description
"[A 60-year-old woman with secondary chronic cluster headache had increased serum ferritin and serum transferrin saturation and was homozygous for the C282Y mutation in the HFE gene, which is indicative of hereditary haemochromatosis.]. 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:12100096
;
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:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:54+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" .
}