@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP364802.RAXK3cf5YMkSdoX3tXEZUqn4si7JmvTxhfTskEUhEeQeY
> .
@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:NP364802.RAXK3cf5YMkSdoX3tXEZUqn4si7JmvTxhfTskEUhEeQeY130_head
{
this:
np:hasAssertion
dgn-np:NP364802.RAXK3cf5YMkSdoX3tXEZUqn4si7JmvTxhfTskEUhEeQeY130_assertion
;
np:hasProvenance
dgn-np:NP364802.RAXK3cf5YMkSdoX3tXEZUqn4si7JmvTxhfTskEUhEeQeY130_provenance
;
np:hasPublicationInfo
dgn-np:NP364802.RAXK3cf5YMkSdoX3tXEZUqn4si7JmvTxhfTskEUhEeQeY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP364802.RAXK3cf5YMkSdoX3tXEZUqn4si7JmvTxhfTskEUhEeQeY130_assertion
a
np:Assertion
.
dgn-np:NP364802.RAXK3cf5YMkSdoX3tXEZUqn4si7JmvTxhfTskEUhEeQeY130_provenance
a
np:Provenance
.
dgn-np:NP364802.RAXK3cf5YMkSdoX3tXEZUqn4si7JmvTxhfTskEUhEeQeY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP364802.RAXK3cf5YMkSdoX3tXEZUqn4si7JmvTxhfTskEUhEeQeY130_assertion
{
miriam-gene:7827
a
ncit:C16612
.
lld:C1458156
a
ncit:C7057
.
dgn-gda:DGN90c8349ec685a4c5f97f997887a60e00
sio:SIO_000628
miriam-gene:7827
,
lld:C1458156
;
a
sio:SIO_001121
.
}
dgn-np:NP364802.RAXK3cf5YMkSdoX3tXEZUqn4si7JmvTxhfTskEUhEeQeY130_provenance
{
dgn-np:NP364802.RAXK3cf5YMkSdoX3tXEZUqn4si7JmvTxhfTskEUhEeQeY130_assertion
dcterms:description
"[Besides better classification of the disease entity, identification of NPHS2 mutations may save some of these patients from unnecessary steroid treatment and also permit the prediction of absence of disease recurrence after kidney transplantation.]. 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:11805166
;
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:NP364802.RAXK3cf5YMkSdoX3tXEZUqn4si7JmvTxhfTskEUhEeQeY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:33+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" .
}