@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1050879.RA-gGpxarGM7MOcfOPfOrN_II7RokBc7DWiyw285w5QZw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1050879.RA-gGpxarGM7MOcfOPfOrN_II7RokBc7DWiyw285w5QZw130_head
{
this:
np:hasAssertion
dgn-np:NP1050879.RA-gGpxarGM7MOcfOPfOrN_II7RokBc7DWiyw285w5QZw130_assertion
;
np:hasProvenance
dgn-np:NP1050879.RA-gGpxarGM7MOcfOPfOrN_II7RokBc7DWiyw285w5QZw130_provenance
;
np:hasPublicationInfo
dgn-np:NP1050879.RA-gGpxarGM7MOcfOPfOrN_II7RokBc7DWiyw285w5QZw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1050879.RA-gGpxarGM7MOcfOPfOrN_II7RokBc7DWiyw285w5QZw130_assertion
a
np:Assertion
.
dgn-np:NP1050879.RA-gGpxarGM7MOcfOPfOrN_II7RokBc7DWiyw285w5QZw130_provenance
a
np:Provenance
.
dgn-np:NP1050879.RA-gGpxarGM7MOcfOPfOrN_II7RokBc7DWiyw285w5QZw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1050879.RA-gGpxarGM7MOcfOPfOrN_II7RokBc7DWiyw285w5QZw130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0392514
a
ncit:C7057
.
dgn-gda:DGN40d97d027c18e1272c060f5475f538fc
sio:SIO_000628
miriam-gene:3077
,
lld:C0392514
;
a
sio:SIO_001121
.
}
dgn-np:NP1050879.RA-gGpxarGM7MOcfOPfOrN_II7RokBc7DWiyw285w5QZw130_provenance
{
dgn-np:NP1050879.RA-gGpxarGM7MOcfOPfOrN_II7RokBc7DWiyw285w5QZw130_assertion
dcterms:description
"[Hereditary hemochromatosis (HH) is a strong risk factor for hepatocellular cancer, and mutations in the HFE gene associated with HH and iron overload may be related to other tumors, but no studies have been reported for gastric cancer (GC).]. 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:23389292
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1050879.RA-gGpxarGM7MOcfOPfOrN_II7RokBc7DWiyw285w5QZw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:42+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}