@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP375966.RAHPfuHoXm3AFU5w_842RWp_XERzxcIMpj5VsrzfOAGJE
> .
@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:NP375966.RAHPfuHoXm3AFU5w_842RWp_XERzxcIMpj5VsrzfOAGJE130_head
{
this:
np:hasAssertion
dgn-np:NP375966.RAHPfuHoXm3AFU5w_842RWp_XERzxcIMpj5VsrzfOAGJE130_assertion
;
np:hasProvenance
dgn-np:NP375966.RAHPfuHoXm3AFU5w_842RWp_XERzxcIMpj5VsrzfOAGJE130_provenance
;
np:hasPublicationInfo
dgn-np:NP375966.RAHPfuHoXm3AFU5w_842RWp_XERzxcIMpj5VsrzfOAGJE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP375966.RAHPfuHoXm3AFU5w_842RWp_XERzxcIMpj5VsrzfOAGJE130_assertion
a
np:Assertion
.
dgn-np:NP375966.RAHPfuHoXm3AFU5w_842RWp_XERzxcIMpj5VsrzfOAGJE130_provenance
a
np:Provenance
.
dgn-np:NP375966.RAHPfuHoXm3AFU5w_842RWp_XERzxcIMpj5VsrzfOAGJE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP375966.RAHPfuHoXm3AFU5w_842RWp_XERzxcIMpj5VsrzfOAGJE130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0023895
a
ncit:C7057
.
dgn-gda:DGN7477e2346ea81655cca9e9873918b540
sio:SIO_000628
miriam-gene:3077
,
lld:C0023895
;
a
sio:SIO_001121
.
}
dgn-np:NP375966.RAHPfuHoXm3AFU5w_842RWp_XERzxcIMpj5VsrzfOAGJE130_provenance
{
dgn-np:NP375966.RAHPfuHoXm3AFU5w_842RWp_XERzxcIMpj5VsrzfOAGJE130_assertion
dcterms:description
"[The recent identification of 2 mutations in the HFE gene related to hereditary haemochromatosis (Cys282Tyr and His63Asp) provided an opportunity to test whether they are associated with hepatic iron accumulation and the activity and severity of liver disease in hepatitis C virus (HCV) infection.]. 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:10692680
;
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:NP375966.RAHPfuHoXm3AFU5w_842RWp_XERzxcIMpj5VsrzfOAGJE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:40+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" .
}