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http://rdf.disgenet.org/nanopublications.trig#NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50
> .
@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:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_assertion
;
np:hasProvenance
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;
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dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_assertion
a
np:Assertion
.
dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_provenance
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np:Provenance
.
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a
np:PublicationInfo
.
}
dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_assertion
{
miriam-gene:5076
a
ncit:C16612
.
lld:C0042580
a
ncit:C7057
.
dgn-gda:DGNa3789ac8147573b236e95042ccb039de
sio:SIO_000628
miriam-gene:5076
,
lld:C0042580
;
a
sio:SIO_001121
.
}
dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_provenance
{
dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_assertion
dcterms:description
"[We were unable to detect linkage to any of the genes and loci and could exclude the GDNF, RET, SLIT2, SPRY1, PAX2, AGTR2, UPK1A and UPK3A genes and the 1p13 and 20p13 loci from linkage to VUR.]. 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:17497182
;
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:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:14+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
> , <
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> , <
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
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dgn-void:disgenetrdf
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"v2.1.0" .
}