@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1059309.RAnnfuFOdQ-wieB5Sdh2szcNojWDODryLi-mv4xuFrawM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP1059309.RAnnfuFOdQ-wieB5Sdh2szcNojWDODryLi-mv4xuFrawM130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1059309.RAnnfuFOdQ-wieB5Sdh2szcNojWDODryLi-mv4xuFrawM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1059309.RAnnfuFOdQ-wieB5Sdh2szcNojWDODryLi-mv4xuFrawM130_assertion
a
np:Assertion
.
dgn-np:NP1059309.RAnnfuFOdQ-wieB5Sdh2szcNojWDODryLi-mv4xuFrawM130_provenance
a
np:Provenance
.
dgn-np:NP1059309.RAnnfuFOdQ-wieB5Sdh2szcNojWDODryLi-mv4xuFrawM130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:5080
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGN249cce718d9a5ecf26be4792774ffe47
sio:SIO_000628
miriam-gene:5080
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP1059309.RAnnfuFOdQ-wieB5Sdh2szcNojWDODryLi-mv4xuFrawM130_provenance
{
dgn-np:NP1059309.RAnnfuFOdQ-wieB5Sdh2szcNojWDODryLi-mv4xuFrawM130_assertion
dcterms:description
"[Human mapping studies have shown that the aniridia (AN2) gene, which is part of the Wilms tumor susceptibility, aniridia, genitourinary abnormalities, and mental retardation (WAGR) complex, is also between FSHB and CAT on human chromosome 11.]. 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:2347591
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1059309.RAnnfuFOdQ-wieB5Sdh2szcNojWDODryLi-mv4xuFrawM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:46+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
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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
"v4.0.0.0" .
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"v4.0.0" .
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