@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP242813.RAFiQyXBoKEwwKLAPXHVPqVrC2jIRO_3c6mi9TfzOxEzE
> .
@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:NP242813.RAFiQyXBoKEwwKLAPXHVPqVrC2jIRO_3c6mi9TfzOxEzE130_head
{
this:
np:hasAssertion
dgn-np:NP242813.RAFiQyXBoKEwwKLAPXHVPqVrC2jIRO_3c6mi9TfzOxEzE130_assertion
;
np:hasProvenance
dgn-np:NP242813.RAFiQyXBoKEwwKLAPXHVPqVrC2jIRO_3c6mi9TfzOxEzE130_provenance
;
np:hasPublicationInfo
dgn-np:NP242813.RAFiQyXBoKEwwKLAPXHVPqVrC2jIRO_3c6mi9TfzOxEzE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP242813.RAFiQyXBoKEwwKLAPXHVPqVrC2jIRO_3c6mi9TfzOxEzE130_assertion
a
np:Assertion
.
dgn-np:NP242813.RAFiQyXBoKEwwKLAPXHVPqVrC2jIRO_3c6mi9TfzOxEzE130_provenance
a
np:Provenance
.
dgn-np:NP242813.RAFiQyXBoKEwwKLAPXHVPqVrC2jIRO_3c6mi9TfzOxEzE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP242813.RAFiQyXBoKEwwKLAPXHVPqVrC2jIRO_3c6mi9TfzOxEzE130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGNc18f2680ee6a8a5f9aedfae14d205605
sio:SIO_000628
miriam-gene:3077
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP242813.RAFiQyXBoKEwwKLAPXHVPqVrC2jIRO_3c6mi9TfzOxEzE130_provenance
{
dgn-np:NP242813.RAFiQyXBoKEwwKLAPXHVPqVrC2jIRO_3c6mi9TfzOxEzE130_assertion
dcterms:description
"[The most frequent causes of death in HH are liver cancer, cirrhosis, cardiomyopathy, and diabetes, but patients who undergo successful iron depletion before the development of cirrhosis or diabetes can have normal survival.]. 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:19034258
;
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:NP242813.RAFiQyXBoKEwwKLAPXHVPqVrC2jIRO_3c6mi9TfzOxEzE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:16+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" .
}