@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo
> .
@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:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_head
{
this:
np:hasAssertion
dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_assertion
;
np:hasProvenance
dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_provenance
;
np:hasPublicationInfo
dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_assertion
a
np:Assertion
.
dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_provenance
a
np:Provenance
.
dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_assertion
{
miriam-gene:6580
a
ncit:C16612
.
lld:C0206698
a
ncit:C7057
.
dgn-gda:DGNb3ae555bd73c4eabc2c773e58a70d4b9
sio:SIO_000628
miriam-gene:6580
,
lld:C0206698
;
a
sio:SIO_001121
.
}
dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_provenance
{
dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_assertion
dcterms:description
"[Conclusion: Development of HCC and CGC is accompanied by the appearance of aberrant OCT1 variants that, together with decreased OCT1 expression, may dramatically affect the ability of sorafenib to reach active intracellular concentrations in these tumors.]. 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:23532667
;
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:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:12+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" .
}