@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_assertion
;
np:hasProvenance
dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_provenance
;
np:hasPublicationInfo
dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_assertion
a
np:Assertion
.
dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_provenance
a
np:Provenance
.
dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_assertion
{
miriam-gene:23158
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN6ef5760934689d8e852c6972d815594a
sio:SIO_000628
miriam-gene:23158
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_provenance
{
dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_assertion
dcterms:description
"[These findings suggest that the common SNPs in the MDR1 gene have no influence on the expression of its transcript in RCC segments as well as in the normal kidney cortex.]. 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:14685825
;
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 .
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dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:04+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
<
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> , <
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" .
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