@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP446955.RAhb2raAHaxgR-NBa4FgXy6Lkg_dFoCAGmI35RM9uxbOU
> .
@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/v3.0.0/void/
> .
dgn-np:NP446955.RAhb2raAHaxgR-NBa4FgXy6Lkg_dFoCAGmI35RM9uxbOU130_head
{
this:
np:hasAssertion
dgn-np:NP446955.RAhb2raAHaxgR-NBa4FgXy6Lkg_dFoCAGmI35RM9uxbOU130_assertion
;
np:hasProvenance
dgn-np:NP446955.RAhb2raAHaxgR-NBa4FgXy6Lkg_dFoCAGmI35RM9uxbOU130_provenance
;
np:hasPublicationInfo
dgn-np:NP446955.RAhb2raAHaxgR-NBa4FgXy6Lkg_dFoCAGmI35RM9uxbOU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP446955.RAhb2raAHaxgR-NBa4FgXy6Lkg_dFoCAGmI35RM9uxbOU130_assertion
a
np:Assertion
.
dgn-np:NP446955.RAhb2raAHaxgR-NBa4FgXy6Lkg_dFoCAGmI35RM9uxbOU130_provenance
a
np:Provenance
.
dgn-np:NP446955.RAhb2raAHaxgR-NBa4FgXy6Lkg_dFoCAGmI35RM9uxbOU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP446955.RAhb2raAHaxgR-NBa4FgXy6Lkg_dFoCAGmI35RM9uxbOU130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0023896
a
ncit:C7057
.
dgn-gda:DGNfe2cbb99605e3026bef381c23209a9b3
sio:SIO_000628
miriam-gene:3077
,
lld:C0023896
;
a
sio:SIO_001122
.
}
dgn-np:NP446955.RAhb2raAHaxgR-NBa4FgXy6Lkg_dFoCAGmI35RM9uxbOU130_provenance
{
dgn-np:NP446955.RAhb2raAHaxgR-NBa4FgXy6Lkg_dFoCAGmI35RM9uxbOU130_assertion
dcterms:description
"[It is less well established that the prevalence of the HFE mutations is increased in alcoholic liver disease and in chronic viral hepatitis, but in both conditions, patients harboring one of these mutations, especially C282Y, are more likely to have advanced hepatic fibrosis or cirrhosis.]. 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:10980924
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP446955.RAhb2raAHaxgR-NBa4FgXy6Lkg_dFoCAGmI35RM9uxbOU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:02+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}