@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP672066.RAOEGEFwplo4fGTSLLVM9V4OU_4X5TQtH7HQnSBOEG1f4
> .
@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:NP672066.RAOEGEFwplo4fGTSLLVM9V4OU_4X5TQtH7HQnSBOEG1f4130_head
{
this:
np:hasAssertion
dgn-np:NP672066.RAOEGEFwplo4fGTSLLVM9V4OU_4X5TQtH7HQnSBOEG1f4130_assertion
;
np:hasProvenance
dgn-np:NP672066.RAOEGEFwplo4fGTSLLVM9V4OU_4X5TQtH7HQnSBOEG1f4130_provenance
;
np:hasPublicationInfo
dgn-np:NP672066.RAOEGEFwplo4fGTSLLVM9V4OU_4X5TQtH7HQnSBOEG1f4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP672066.RAOEGEFwplo4fGTSLLVM9V4OU_4X5TQtH7HQnSBOEG1f4130_assertion
a
np:Assertion
.
dgn-np:NP672066.RAOEGEFwplo4fGTSLLVM9V4OU_4X5TQtH7HQnSBOEG1f4130_provenance
a
np:Provenance
.
dgn-np:NP672066.RAOEGEFwplo4fGTSLLVM9V4OU_4X5TQtH7HQnSBOEG1f4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP672066.RAOEGEFwplo4fGTSLLVM9V4OU_4X5TQtH7HQnSBOEG1f4130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0268063
a
ncit:C7057
.
dgn-gda:DGN601a92f6b53755b1d07990d18249bff7
sio:SIO_000628
miriam-gene:3077
,
lld:C0268063
;
a
sio:SIO_001121
.
}
dgn-np:NP672066.RAOEGEFwplo4fGTSLLVM9V4OU_4X5TQtH7HQnSBOEG1f4130_provenance
{
dgn-np:NP672066.RAOEGEFwplo4fGTSLLVM9V4OU_4X5TQtH7HQnSBOEG1f4130_assertion
dcterms:description
"[Although most iron overload cases in African Americans bear more resemblance to cases of African iron overload than to those of Caucasian hemochromatosis, rare cases resembling Caucasian hemochromatosis have been observed in African Americans.]. 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:11763282
;
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:NP672066.RAOEGEFwplo4fGTSLLVM9V4OU_4X5TQtH7HQnSBOEG1f4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:45+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" .
}