@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP738115.RAnwe4d_qEqtFCCwtBnbz2Q4JyW43Z-cvizmhdLmbrK8c
> .
@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:NP738115.RAnwe4d_qEqtFCCwtBnbz2Q4JyW43Z-cvizmhdLmbrK8c130_head
{
this:
np:hasAssertion
dgn-np:NP738115.RAnwe4d_qEqtFCCwtBnbz2Q4JyW43Z-cvizmhdLmbrK8c130_assertion
;
np:hasProvenance
dgn-np:NP738115.RAnwe4d_qEqtFCCwtBnbz2Q4JyW43Z-cvizmhdLmbrK8c130_provenance
;
np:hasPublicationInfo
dgn-np:NP738115.RAnwe4d_qEqtFCCwtBnbz2Q4JyW43Z-cvizmhdLmbrK8c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP738115.RAnwe4d_qEqtFCCwtBnbz2Q4JyW43Z-cvizmhdLmbrK8c130_assertion
a
np:Assertion
.
dgn-np:NP738115.RAnwe4d_qEqtFCCwtBnbz2Q4JyW43Z-cvizmhdLmbrK8c130_provenance
a
np:Provenance
.
dgn-np:NP738115.RAnwe4d_qEqtFCCwtBnbz2Q4JyW43Z-cvizmhdLmbrK8c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP738115.RAnwe4d_qEqtFCCwtBnbz2Q4JyW43Z-cvizmhdLmbrK8c130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0392514
a
ncit:C7057
.
dgn-gda:DGN26068a66e7c80520b35ef2f8ea073dc4
sio:SIO_000628
miriam-gene:3077
,
lld:C0392514
;
a
sio:SIO_001121
.
}
dgn-np:NP738115.RAnwe4d_qEqtFCCwtBnbz2Q4JyW43Z-cvizmhdLmbrK8c130_provenance
{
dgn-np:NP738115.RAnwe4d_qEqtFCCwtBnbz2Q4JyW43Z-cvizmhdLmbrK8c130_assertion
dcterms:description
"[The inclusion of iron studies during routine clinical visits, coupled with the availability of HFE genotyping for family and population studies, should facilitate the early detection of hereditary haemochromatosis in Romania.]. 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:19433916
;
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:NP738115.RAnwe4d_qEqtFCCwtBnbz2Q4JyW43Z-cvizmhdLmbrK8c130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:19+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" .
}