@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0
> .
@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:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_head
{
this:
np:hasAssertion
dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_assertion
;
np:hasProvenance
dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_provenance
;
np:hasPublicationInfo
dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_assertion
a
np:Assertion
.
dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_provenance
a
np:Provenance
.
dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN547343f88f0f66dc7129687f77cab962
sio:SIO_000628
miriam-gene:3077
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_provenance
{
dgn-np:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_assertion
dcterms:description
"[A total of 87 persons with hemochromatosis (patients) (39 women, 48 men), who underwent HFE genotyping, and 50 persons with hypertension (controls) (22 women, 28 men), who had not undergone HFE genotyping, completed a structured interview in which they reported attitudes about benefits and disadvantages of genetic testing and their understanding of genetics and hemochromatosis.]. 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:15345103
;
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:NP741464.RAJZ_zalNgINBF8_9zjF4uUIwllpjLZeDznmkNjwwypd0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:30+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" .
}