@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP793667.RAeewm2VYCTjs8LTU9pMJPIU8NCUTOsVhpKxjgB8wcGas
> .
@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:NP793667.RAeewm2VYCTjs8LTU9pMJPIU8NCUTOsVhpKxjgB8wcGas130_head
{
this:
np:hasAssertion
dgn-np:NP793667.RAeewm2VYCTjs8LTU9pMJPIU8NCUTOsVhpKxjgB8wcGas130_assertion
;
np:hasProvenance
dgn-np:NP793667.RAeewm2VYCTjs8LTU9pMJPIU8NCUTOsVhpKxjgB8wcGas130_provenance
;
np:hasPublicationInfo
dgn-np:NP793667.RAeewm2VYCTjs8LTU9pMJPIU8NCUTOsVhpKxjgB8wcGas130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP793667.RAeewm2VYCTjs8LTU9pMJPIU8NCUTOsVhpKxjgB8wcGas130_assertion
a
np:Assertion
.
dgn-np:NP793667.RAeewm2VYCTjs8LTU9pMJPIU8NCUTOsVhpKxjgB8wcGas130_provenance
a
np:Provenance
.
dgn-np:NP793667.RAeewm2VYCTjs8LTU9pMJPIU8NCUTOsVhpKxjgB8wcGas130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP793667.RAeewm2VYCTjs8LTU9pMJPIU8NCUTOsVhpKxjgB8wcGas130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0018995
a
ncit:C7057
.
dgn-gda:DGN81e8529281f0ff87adb4f28fe65f78c5
sio:SIO_000628
miriam-gene:3126
,
lld:C0018995
;
a
sio:SIO_001121
.
}
dgn-np:NP793667.RAeewm2VYCTjs8LTU9pMJPIU8NCUTOsVhpKxjgB8wcGas130_provenance
{
dgn-np:NP793667.RAeewm2VYCTjs8LTU9pMJPIU8NCUTOsVhpKxjgB8wcGas130_assertion
dcterms:description
"[To assess the clinical value of human leukocyte antigen typing in the diagnosis and management of hereditary hemochromatosis, 105 siblings of 35 proband cases of hemochromatosis were retrospectively analyzed to study whether the exclusion of human leukocyte antigen typing would have adversely affected management.]. 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:1735529
;
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:NP793667.RAeewm2VYCTjs8LTU9pMJPIU8NCUTOsVhpKxjgB8wcGas130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:07+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" .
}