@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP359304.RAqOGSCHvhP-ZAFOv4Qy_EMr0YbgX7x-LUEKKQ-3oO45Y
> .
@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:NP359304.RAqOGSCHvhP-ZAFOv4Qy_EMr0YbgX7x-LUEKKQ-3oO45Y130_head
{
this:
np:hasAssertion
dgn-np:NP359304.RAqOGSCHvhP-ZAFOv4Qy_EMr0YbgX7x-LUEKKQ-3oO45Y130_assertion
;
np:hasProvenance
dgn-np:NP359304.RAqOGSCHvhP-ZAFOv4Qy_EMr0YbgX7x-LUEKKQ-3oO45Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP359304.RAqOGSCHvhP-ZAFOv4Qy_EMr0YbgX7x-LUEKKQ-3oO45Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP359304.RAqOGSCHvhP-ZAFOv4Qy_EMr0YbgX7x-LUEKKQ-3oO45Y130_assertion
a
np:Assertion
.
dgn-np:NP359304.RAqOGSCHvhP-ZAFOv4Qy_EMr0YbgX7x-LUEKKQ-3oO45Y130_provenance
a
np:Provenance
.
dgn-np:NP359304.RAqOGSCHvhP-ZAFOv4Qy_EMr0YbgX7x-LUEKKQ-3oO45Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP359304.RAqOGSCHvhP-ZAFOv4Qy_EMr0YbgX7x-LUEKKQ-3oO45Y130_assertion
{
miriam-gene:4868
a
ncit:C16612
.
lld:C0027726
a
ncit:C7057
.
dgn-gda:DGN4ab716ebe0ef62bef159ccbfe40c99d9
sio:SIO_000628
miriam-gene:4868
,
lld:C0027726
;
a
sio:SIO_001121
.
}
dgn-np:NP359304.RAqOGSCHvhP-ZAFOv4Qy_EMr0YbgX7x-LUEKKQ-3oO45Y130_provenance
{
dgn-np:NP359304.RAqOGSCHvhP-ZAFOv4Qy_EMr0YbgX7x-LUEKKQ-3oO45Y130_assertion
dcterms:description
"[To determine the frequency of inherited NS, 62 cases (representing 49 families with NS) from Saudi Arabia were screened for mutations in NPHS1, NPHS2, LAMB2, PLCE1, CD2AP, MYO1E, WT1, PTPRO and Nei endonuclease VIII-like 1 (NEIL1).]. 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:23595123
;
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:NP359304.RAqOGSCHvhP-ZAFOv4Qy_EMr0YbgX7x-LUEKKQ-3oO45Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:30+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" .
}