@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP466796.RAsmOMll_UkmSrBzqH-XnXPpEFLZN_waUQSXPscqrMtfU
> .
@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:NP466796.RAsmOMll_UkmSrBzqH-XnXPpEFLZN_waUQSXPscqrMtfU130_head
{
this:
np:hasAssertion
dgn-np:NP466796.RAsmOMll_UkmSrBzqH-XnXPpEFLZN_waUQSXPscqrMtfU130_assertion
;
np:hasProvenance
dgn-np:NP466796.RAsmOMll_UkmSrBzqH-XnXPpEFLZN_waUQSXPscqrMtfU130_provenance
;
np:hasPublicationInfo
dgn-np:NP466796.RAsmOMll_UkmSrBzqH-XnXPpEFLZN_waUQSXPscqrMtfU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP466796.RAsmOMll_UkmSrBzqH-XnXPpEFLZN_waUQSXPscqrMtfU130_assertion
a
np:Assertion
.
dgn-np:NP466796.RAsmOMll_UkmSrBzqH-XnXPpEFLZN_waUQSXPscqrMtfU130_provenance
a
np:Provenance
.
dgn-np:NP466796.RAsmOMll_UkmSrBzqH-XnXPpEFLZN_waUQSXPscqrMtfU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP466796.RAsmOMll_UkmSrBzqH-XnXPpEFLZN_waUQSXPscqrMtfU130_assertion
{
miriam-gene:2332
a
ncit:C16612
.
lld:C0026351
a
ncit:C7057
.
dgn-gda:DGNe372d04c5f21e07ed6fa84bdd083af6a
sio:SIO_000628
miriam-gene:2332
,
lld:C0026351
;
a
sio:SIO_001121
.
}
dgn-np:NP466796.RAsmOMll_UkmSrBzqH-XnXPpEFLZN_waUQSXPscqrMtfU130_provenance
{
dgn-np:NP466796.RAsmOMll_UkmSrBzqH-XnXPpEFLZN_waUQSXPscqrMtfU130_assertion
dcterms:description
"[A survey of children attending schools for the moderately or the mildly mentally handicapped has shown that two out of 25 boys and two out of 22 girls with idiopathic moderate mental retardation had the Martin-Bell syndrome, while none of 75 boys and one out of 51 girls with mild mental retardation were FRAXA positive.]. 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:1800751
;
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:NP466796.RAsmOMll_UkmSrBzqH-XnXPpEFLZN_waUQSXPscqrMtfU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:40+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: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" .
}