@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1371956.RAavxOj8zNk7LhEyDmLq25mLiFRRk1T8pIfkf15UtL_eo
> .
@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/
> .
dgn-np:NP1371956.RAavxOj8zNk7LhEyDmLq25mLiFRRk1T8pIfkf15UtL_eo130_head
{
this:
np:hasAssertion
dgn-np:NP1371956.RAavxOj8zNk7LhEyDmLq25mLiFRRk1T8pIfkf15UtL_eo130_assertion
;
np:hasProvenance
dgn-np:NP1371956.RAavxOj8zNk7LhEyDmLq25mLiFRRk1T8pIfkf15UtL_eo130_provenance
;
np:hasPublicationInfo
dgn-np:NP1371956.RAavxOj8zNk7LhEyDmLq25mLiFRRk1T8pIfkf15UtL_eo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1371956.RAavxOj8zNk7LhEyDmLq25mLiFRRk1T8pIfkf15UtL_eo130_assertion
a
np:Assertion
.
dgn-np:NP1371956.RAavxOj8zNk7LhEyDmLq25mLiFRRk1T8pIfkf15UtL_eo130_provenance
a
np:Provenance
.
dgn-np:NP1371956.RAavxOj8zNk7LhEyDmLq25mLiFRRk1T8pIfkf15UtL_eo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1371956.RAavxOj8zNk7LhEyDmLq25mLiFRRk1T8pIfkf15UtL_eo130_assertion
{
miriam-gene:7490
a
ncit:C16612
.
lld:C0027708
a
ncit:C7057
.
dgn-gda:DGN2aaeca1a2b329788ff8ca9df66b190b4
sio:SIO_000628
miriam-gene:7490
,
lld:C0027708
;
a
sio:SIO_001121
.
}
dgn-np:NP1371956.RAavxOj8zNk7LhEyDmLq25mLiFRRk1T8pIfkf15UtL_eo130_provenance
{
dgn-np:NP1371956.RAavxOj8zNk7LhEyDmLq25mLiFRRk1T8pIfkf15UtL_eo130_assertion
dcterms:description
"[They were examined because they had either isolated sporadic or familial aniridia, or aniridia with one or more of the WAGR (Wilms' tumour, aniridia, genital anomalies, and mental retardation) syndrome anomalies.]. 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:9132491
;
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:NP1371956.RAavxOj8zNk7LhEyDmLq25mLiFRRk1T8pIfkf15UtL_eo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:08+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}