@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY
> .
@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:NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_head
{
this:
np:hasAssertion
dgn-np:NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_assertion
;
np:hasProvenance
dgn-np:NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_provenance
;
np:hasPublicationInfo
dgn-np:NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_assertion
a
np:Assertion
.
dgn-np:NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_provenance
a
np:Provenance
.
dgn-np:NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_assertion
{
miriam-gene:2477
a
ncit:C16612
.
lld:C1136249
a
ncit:C7057
.
dgn-gda:DGNb8ffe1aa53ba3558e7b675e4e8534921
sio:SIO_000628
miriam-gene:2477
,
lld:C1136249
;
a
sio:SIO_001121
.
}
dgn-np:NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_provenance
{
dgn-np:NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_assertion
dcterms:description
"[In order to evaluate the frequency of ARX mutation in XLMR, we performed mutational analysis of ARX in 165 mentally retarded probands negative for FRAXA and belonging to families in which the condition segregates as an X-linked condition.]. 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:16523516
;
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:NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:31+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" .
}