@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP282062.RArYEKRoqrnjgs-O71QiCligZs3R_GImRzmLgvfREdQMI
> .
@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:NP282062.RArYEKRoqrnjgs-O71QiCligZs3R_GImRzmLgvfREdQMI130_head
{
this:
np:hasAssertion
dgn-np:NP282062.RArYEKRoqrnjgs-O71QiCligZs3R_GImRzmLgvfREdQMI130_assertion
;
np:hasProvenance
dgn-np:NP282062.RArYEKRoqrnjgs-O71QiCligZs3R_GImRzmLgvfREdQMI130_provenance
;
np:hasPublicationInfo
dgn-np:NP282062.RArYEKRoqrnjgs-O71QiCligZs3R_GImRzmLgvfREdQMI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP282062.RArYEKRoqrnjgs-O71QiCligZs3R_GImRzmLgvfREdQMI130_assertion
a
np:Assertion
.
dgn-np:NP282062.RArYEKRoqrnjgs-O71QiCligZs3R_GImRzmLgvfREdQMI130_provenance
a
np:Provenance
.
dgn-np:NP282062.RArYEKRoqrnjgs-O71QiCligZs3R_GImRzmLgvfREdQMI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP282062.RArYEKRoqrnjgs-O71QiCligZs3R_GImRzmLgvfREdQMI130_assertion
{
miriam-gene:51750
a
ncit:C16612
.
lld:C0019189
a
ncit:C7057
.
dgn-gda:DGNd6f6e5f76f3111b814bed689b385a632
sio:SIO_000628
miriam-gene:51750
,
lld:C0019189
;
a
sio:SIO_001121
.
}
dgn-np:NP282062.RArYEKRoqrnjgs-O71QiCligZs3R_GImRzmLgvfREdQMI130_provenance
{
dgn-np:NP282062.RArYEKRoqrnjgs-O71QiCligZs3R_GImRzmLgvfREdQMI130_assertion
dcterms:description
"[Hepatitis C virus (HCV) has been identified as one of the major risk factors for type II mixed cryoglobulinemia (MC), during the clinical evolution of chronic hepatitis, which may lead to development of B cell non-Hodgkin's lymphoma (NHL).]. 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:23028651
;
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:NP282062.RArYEKRoqrnjgs-O71QiCligZs3R_GImRzmLgvfREdQMI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:39+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" .
}