@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo
> .
@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:NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_head
{
this:
np:hasAssertion
dgn-np:NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_assertion
;
np:hasProvenance
dgn-np:NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_provenance
;
np:hasPublicationInfo
dgn-np:NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_assertion
a
np:Assertion
.
dgn-np:NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_provenance
a
np:Provenance
.
dgn-np:NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0018995
a
ncit:C7057
.
dgn-gda:DGN0cb68cec7315214adba90b0431023f69
sio:SIO_000628
miriam-gene:3077
,
lld:C0018995
;
a
sio:SIO_001122
.
}
dgn-np:NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_provenance
{
dgn-np:NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_assertion
dcterms:description
"[To study the prevalence of homozygotic H63D mutation in patients with phenotypic hemochromatosis (PH) and to compare the results with those of the general population and with patients with porphyria cutanea tarda (PCT) in the Basque Country, Spain.]. 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:20594259
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:09+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" .
}