@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP254719.RA1n0O44dIbn3aFtgZdPPi9KJR60Thj9dDQwZtyV6xUDA
> .
@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:NP254719.RA1n0O44dIbn3aFtgZdPPi9KJR60Thj9dDQwZtyV6xUDA130_head
{
this:
np:hasAssertion
dgn-np:NP254719.RA1n0O44dIbn3aFtgZdPPi9KJR60Thj9dDQwZtyV6xUDA130_assertion
;
np:hasProvenance
dgn-np:NP254719.RA1n0O44dIbn3aFtgZdPPi9KJR60Thj9dDQwZtyV6xUDA130_provenance
;
np:hasPublicationInfo
dgn-np:NP254719.RA1n0O44dIbn3aFtgZdPPi9KJR60Thj9dDQwZtyV6xUDA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP254719.RA1n0O44dIbn3aFtgZdPPi9KJR60Thj9dDQwZtyV6xUDA130_assertion
a
np:Assertion
.
dgn-np:NP254719.RA1n0O44dIbn3aFtgZdPPi9KJR60Thj9dDQwZtyV6xUDA130_provenance
a
np:Provenance
.
dgn-np:NP254719.RA1n0O44dIbn3aFtgZdPPi9KJR60Thj9dDQwZtyV6xUDA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP254719.RA1n0O44dIbn3aFtgZdPPi9KJR60Thj9dDQwZtyV6xUDA130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0279000
a
ncit:C7057
.
dgn-gda:DGN8c1295313f6e248ffea7d4a9843ef93f
sio:SIO_000628
miriam-gene:3077
,
lld:C0279000
;
a
sio:SIO_001121
.
}
dgn-np:NP254719.RA1n0O44dIbn3aFtgZdPPi9KJR60Thj9dDQwZtyV6xUDA130_provenance
{
dgn-np:NP254719.RA1n0O44dIbn3aFtgZdPPi9KJR60Thj9dDQwZtyV6xUDA130_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:NP254719.RA1n0O44dIbn3aFtgZdPPi9KJR60Thj9dDQwZtyV6xUDA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:22+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" .
}