@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP382385.RAu_2STqya395NNYMeuKVCP6odjZsHMI6cF6bagk6Rwdw
> .
@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:NP382385.RAu_2STqya395NNYMeuKVCP6odjZsHMI6cF6bagk6Rwdw130_head
{
this:
np:hasAssertion
dgn-np:NP382385.RAu_2STqya395NNYMeuKVCP6odjZsHMI6cF6bagk6Rwdw130_assertion
;
np:hasProvenance
dgn-np:NP382385.RAu_2STqya395NNYMeuKVCP6odjZsHMI6cF6bagk6Rwdw130_provenance
;
np:hasPublicationInfo
dgn-np:NP382385.RAu_2STqya395NNYMeuKVCP6odjZsHMI6cF6bagk6Rwdw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP382385.RAu_2STqya395NNYMeuKVCP6odjZsHMI6cF6bagk6Rwdw130_assertion
a
np:Assertion
.
dgn-np:NP382385.RAu_2STqya395NNYMeuKVCP6odjZsHMI6cF6bagk6Rwdw130_provenance
a
np:Provenance
.
dgn-np:NP382385.RAu_2STqya395NNYMeuKVCP6odjZsHMI6cF6bagk6Rwdw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP382385.RAu_2STqya395NNYMeuKVCP6odjZsHMI6cF6bagk6Rwdw130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0022661
a
ncit:C7057
.
dgn-gda:DGNe2147482812ff85650610de323b084d4
sio:SIO_000628
miriam-gene:4846
,
lld:C0022661
;
a
sio:SIO_001121
.
}
dgn-np:NP382385.RAu_2STqya395NNYMeuKVCP6odjZsHMI6cF6bagk6Rwdw130_provenance
{
dgn-np:NP382385.RAu_2STqya395NNYMeuKVCP6odjZsHMI6cF6bagk6Rwdw130_assertion
dcterms:description
"[This fact may be important for the development of atherosclerotic lesions during chronic renal failure and is in accordance with recently published studies showing that under conditions with decreased constitutive NOS activity, iNOS might substitute the synthesis of NO.]. 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:11168974
;
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:NP382385.RAu_2STqya395NNYMeuKVCP6odjZsHMI6cF6bagk6Rwdw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:46+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" .
}