@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP857925.RAmxF2n-j27OFTW0VctNBkas8u72SayFcJq5Ympvqg9Yw
> .
@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:NP857925.RAmxF2n-j27OFTW0VctNBkas8u72SayFcJq5Ympvqg9Yw130_head
{
this:
np:hasAssertion
dgn-np:NP857925.RAmxF2n-j27OFTW0VctNBkas8u72SayFcJq5Ympvqg9Yw130_assertion
;
np:hasProvenance
dgn-np:NP857925.RAmxF2n-j27OFTW0VctNBkas8u72SayFcJq5Ympvqg9Yw130_provenance
;
np:hasPublicationInfo
dgn-np:NP857925.RAmxF2n-j27OFTW0VctNBkas8u72SayFcJq5Ympvqg9Yw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP857925.RAmxF2n-j27OFTW0VctNBkas8u72SayFcJq5Ympvqg9Yw130_assertion
a
np:Assertion
.
dgn-np:NP857925.RAmxF2n-j27OFTW0VctNBkas8u72SayFcJq5Ympvqg9Yw130_provenance
a
np:Provenance
.
dgn-np:NP857925.RAmxF2n-j27OFTW0VctNBkas8u72SayFcJq5Ympvqg9Yw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP857925.RAmxF2n-j27OFTW0VctNBkas8u72SayFcJq5Ympvqg9Yw130_assertion
{
miriam-gene:282617
a
ncit:C16612
.
lld:C0524910
a
ncit:C7057
.
dgn-gda:DGNa31c93ce2ae2db2d15f2a32540640663
sio:SIO_000628
miriam-gene:282617
,
lld:C0524910
;
a
sio:SIO_001122
.
}
dgn-np:NP857925.RAmxF2n-j27OFTW0VctNBkas8u72SayFcJq5Ympvqg9Yw130_provenance
{
dgn-np:NP857925.RAmxF2n-j27OFTW0VctNBkas8u72SayFcJq5Ympvqg9Yw130_assertion
dcterms:description
"[IL-28B rs12979860 C/T polymorphism T allele is more prevalent in patients with viral cirrhosis due to HCV in comparison to other aetiologies and to patients with mild chronic hepatitis C. Among OLT patients, carriage of this allele seems to augment the risk of developing HCC.]. 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:21146242
;
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:NP857925.RAmxF2n-j27OFTW0VctNBkas8u72SayFcJq5Ympvqg9Yw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:13+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" .
}