@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP410416.RA3U6pZQ1DrE4Qvknno9MGifuj3m2Zd6a643c9VPugN-4
> .
@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:NP410416.RA3U6pZQ1DrE4Qvknno9MGifuj3m2Zd6a643c9VPugN-4130_head
{
this:
np:hasAssertion
dgn-np:NP410416.RA3U6pZQ1DrE4Qvknno9MGifuj3m2Zd6a643c9VPugN-4130_assertion
;
np:hasProvenance
dgn-np:NP410416.RA3U6pZQ1DrE4Qvknno9MGifuj3m2Zd6a643c9VPugN-4130_provenance
;
np:hasPublicationInfo
dgn-np:NP410416.RA3U6pZQ1DrE4Qvknno9MGifuj3m2Zd6a643c9VPugN-4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP410416.RA3U6pZQ1DrE4Qvknno9MGifuj3m2Zd6a643c9VPugN-4130_assertion
a
np:Assertion
.
dgn-np:NP410416.RA3U6pZQ1DrE4Qvknno9MGifuj3m2Zd6a643c9VPugN-4130_provenance
a
np:Provenance
.
dgn-np:NP410416.RA3U6pZQ1DrE4Qvknno9MGifuj3m2Zd6a643c9VPugN-4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP410416.RA3U6pZQ1DrE4Qvknno9MGifuj3m2Zd6a643c9VPugN-4130_assertion
{
miriam-gene:6716
a
ncit:C16612
.
lld:C0524910
a
ncit:C7057
.
dgn-gda:DGN5a62c728fd3d3524a2f254405755fd61
sio:SIO_000628
miriam-gene:6716
,
lld:C0524910
;
a
sio:SIO_001121
.
}
dgn-np:NP410416.RA3U6pZQ1DrE4Qvknno9MGifuj3m2Zd6a643c9VPugN-4130_provenance
{
dgn-np:NP410416.RA3U6pZQ1DrE4Qvknno9MGifuj3m2Zd6a643c9VPugN-4130_assertion
dcterms:description
"[As progression of chronic hepatitis C and risk of liver cancer is higher in males than in females, we evaluated whether the polymorphisms of three enzymes participating in the pathway of estrogen and androgen biosynthesis and inactivation, 5alpha-reductase type II (SRD5A2), cytochrome P450c17alpha (CYP17) and catechol-O-methyltransferase (COMT), might affect the expression of hepatitis C virus (HCV)-related liver disease.]. 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:12971967
;
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:NP410416.RA3U6pZQ1DrE4Qvknno9MGifuj3m2Zd6a643c9VPugN-4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:04+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" .
}