@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP412996.RAj5Wc29IiVwAtq0diNfEQ4X3dh4IA4EbD7czG_fWWVu4
> .
@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/v3.0.0/void/
> .
dgn-np:NP412996.RAj5Wc29IiVwAtq0diNfEQ4X3dh4IA4EbD7czG_fWWVu4130_head
{
this:
np:hasAssertion
dgn-np:NP412996.RAj5Wc29IiVwAtq0diNfEQ4X3dh4IA4EbD7czG_fWWVu4130_assertion
;
np:hasProvenance
dgn-np:NP412996.RAj5Wc29IiVwAtq0diNfEQ4X3dh4IA4EbD7czG_fWWVu4130_provenance
;
np:hasPublicationInfo
dgn-np:NP412996.RAj5Wc29IiVwAtq0diNfEQ4X3dh4IA4EbD7czG_fWWVu4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP412996.RAj5Wc29IiVwAtq0diNfEQ4X3dh4IA4EbD7czG_fWWVu4130_assertion
a
np:Assertion
.
dgn-np:NP412996.RAj5Wc29IiVwAtq0diNfEQ4X3dh4IA4EbD7czG_fWWVu4130_provenance
a
np:Provenance
.
dgn-np:NP412996.RAj5Wc29IiVwAtq0diNfEQ4X3dh4IA4EbD7czG_fWWVu4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP412996.RAj5Wc29IiVwAtq0diNfEQ4X3dh4IA4EbD7czG_fWWVu4130_assertion
{
miriam-gene:2488
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGN2ab9d97ecfbdf965de1c76fe3f8cbf5b
sio:SIO_000628
miriam-gene:2488
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP412996.RAj5Wc29IiVwAtq0diNfEQ4X3dh4IA4EbD7czG_fWWVu4130_provenance
{
dgn-np:NP412996.RAj5Wc29IiVwAtq0diNfEQ4X3dh4IA4EbD7czG_fWWVu4130_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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP412996.RAj5Wc29IiVwAtq0diNfEQ4X3dh4IA4EbD7czG_fWWVu4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:40+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}