@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP659103.RAHa2XBMBCp5CR7evsbbK_J_WReSfF2ernqKIfBt_vwZs
> .
@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:NP659103.RAHa2XBMBCp5CR7evsbbK_J_WReSfF2ernqKIfBt_vwZs130_head
{
this:
np:hasAssertion
dgn-np:NP659103.RAHa2XBMBCp5CR7evsbbK_J_WReSfF2ernqKIfBt_vwZs130_assertion
;
np:hasProvenance
dgn-np:NP659103.RAHa2XBMBCp5CR7evsbbK_J_WReSfF2ernqKIfBt_vwZs130_provenance
;
np:hasPublicationInfo
dgn-np:NP659103.RAHa2XBMBCp5CR7evsbbK_J_WReSfF2ernqKIfBt_vwZs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP659103.RAHa2XBMBCp5CR7evsbbK_J_WReSfF2ernqKIfBt_vwZs130_assertion
a
np:Assertion
.
dgn-np:NP659103.RAHa2XBMBCp5CR7evsbbK_J_WReSfF2ernqKIfBt_vwZs130_provenance
a
np:Provenance
.
dgn-np:NP659103.RAHa2XBMBCp5CR7evsbbK_J_WReSfF2ernqKIfBt_vwZs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP659103.RAHa2XBMBCp5CR7evsbbK_J_WReSfF2ernqKIfBt_vwZs130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0023890
a
ncit:C7057
.
dgn-gda:DGNf72b0e03cfa5bf5372ed1cf25ab49fba
sio:SIO_000628
miriam-gene:348
,
lld:C0023890
;
a
sio:SIO_001121
.
}
dgn-np:NP659103.RAHa2XBMBCp5CR7evsbbK_J_WReSfF2ernqKIfBt_vwZs130_provenance
{
dgn-np:NP659103.RAHa2XBMBCp5CR7evsbbK_J_WReSfF2ernqKIfBt_vwZs130_assertion
dcterms:description
"[The overall apoE allele frequencies of patients with liver disease not caused by HCV were similar to those of the total HCV group and in contrast to the HCV patients, the apoE allele frequencies were similar in those patients with no or mild fibrosis as compared with those with bridging 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:12143056
;
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:NP659103.RAHa2XBMBCp5CR7evsbbK_J_WReSfF2ernqKIfBt_vwZs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:38+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" .
}