@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI
> .
@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:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_head
{
this:
np:hasAssertion
dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_assertion
;
np:hasProvenance
dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_provenance
;
np:hasPublicationInfo
dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_assertion
a
np:Assertion
.
dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_provenance
a
np:Provenance
.
dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_assertion
{
miriam-gene:2334
a
ncit:C16612
.
lld:C2752082
a
ncit:C7057
.
dgn-gda:DGNba6b5dd61b3e538c5f4ec3366228db4c
sio:SIO_000628
miriam-gene:2334
,
lld:C2752082
;
a
sio:SIO_001121
.
}
dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_provenance
{
dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_assertion
dcterms:description
"[Since these activities likely extend to the entire ALF protein family, this study also significantly inputs our understanding of the molecular basis of FRAXE mental retardation syndrome in which FMR2 expression is silenced.]. 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:17135274
;
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:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:27+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" .
}