@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP447315.RAfj4-M-Rrl2USkmEtiGyCgEmgn0kDl85NXjgVVd-wIus
> .
@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/v3.0.0/void/
> .
dgn-np:NP447315.RAfj4-M-Rrl2USkmEtiGyCgEmgn0kDl85NXjgVVd-wIus130_head
{
this:
np:hasAssertion
dgn-np:NP447315.RAfj4-M-Rrl2USkmEtiGyCgEmgn0kDl85NXjgVVd-wIus130_assertion
;
np:hasProvenance
dgn-np:NP447315.RAfj4-M-Rrl2USkmEtiGyCgEmgn0kDl85NXjgVVd-wIus130_provenance
;
np:hasPublicationInfo
dgn-np:NP447315.RAfj4-M-Rrl2USkmEtiGyCgEmgn0kDl85NXjgVVd-wIus130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP447315.RAfj4-M-Rrl2USkmEtiGyCgEmgn0kDl85NXjgVVd-wIus130_assertion
a
np:Assertion
.
dgn-np:NP447315.RAfj4-M-Rrl2USkmEtiGyCgEmgn0kDl85NXjgVVd-wIus130_provenance
a
np:Provenance
.
dgn-np:NP447315.RAfj4-M-Rrl2USkmEtiGyCgEmgn0kDl85NXjgVVd-wIus130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP447315.RAfj4-M-Rrl2USkmEtiGyCgEmgn0kDl85NXjgVVd-wIus130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C1858664
a
ncit:C7057
.
dgn-gda:DGNcb3f17255d9be084c281f5d2dba06660
sio:SIO_000628
miriam-gene:3077
,
lld:C1858664
;
a
sio:SIO_001122
.
}
dgn-np:NP447315.RAfj4-M-Rrl2USkmEtiGyCgEmgn0kDl85NXjgVVd-wIus130_provenance
{
dgn-np:NP447315.RAfj4-M-Rrl2USkmEtiGyCgEmgn0kDl85NXjgVVd-wIus130_assertion
dcterms:description
"[By contrast, the frequencies of the common H63D mutation did not differ, and the allele frequencies of the less frequently observed sequence deviations as substitution S65C in the HFE gene and mutation Y250X in the TFR2 gene underlying hemochromatosis type 3 (HFE3) were < 0.02 both in PCT patients and controls.]. 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:17298224
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP447315.RAfj4-M-Rrl2USkmEtiGyCgEmgn0kDl85NXjgVVd-wIus130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:02+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}