@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP581379.RAYJWf36_uKWtTIksR3Xgj4KxiXm-Pij6E-7mEbxl_ans
> .
@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:NP581379.RAYJWf36_uKWtTIksR3Xgj4KxiXm-Pij6E-7mEbxl_ans130_head
{
this:
np:hasAssertion
dgn-np:NP581379.RAYJWf36_uKWtTIksR3Xgj4KxiXm-Pij6E-7mEbxl_ans130_assertion
;
np:hasProvenance
dgn-np:NP581379.RAYJWf36_uKWtTIksR3Xgj4KxiXm-Pij6E-7mEbxl_ans130_provenance
;
np:hasPublicationInfo
dgn-np:NP581379.RAYJWf36_uKWtTIksR3Xgj4KxiXm-Pij6E-7mEbxl_ans130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP581379.RAYJWf36_uKWtTIksR3Xgj4KxiXm-Pij6E-7mEbxl_ans130_assertion
a
np:Assertion
.
dgn-np:NP581379.RAYJWf36_uKWtTIksR3Xgj4KxiXm-Pij6E-7mEbxl_ans130_provenance
a
np:Provenance
.
dgn-np:NP581379.RAYJWf36_uKWtTIksR3Xgj4KxiXm-Pij6E-7mEbxl_ans130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP581379.RAYJWf36_uKWtTIksR3Xgj4KxiXm-Pij6E-7mEbxl_ans130_assertion
{
miriam-gene:55998
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGN4a0ee888a705191bfba57879533d3708
sio:SIO_000628
miriam-gene:55998
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP581379.RAYJWf36_uKWtTIksR3Xgj4KxiXm-Pij6E-7mEbxl_ans130_provenance
{
dgn-np:NP581379.RAYJWf36_uKWtTIksR3Xgj4KxiXm-Pij6E-7mEbxl_ans130_assertion
dcterms:description
"[Among them, the NXF5 gene has already been linked to mental retardation whereas NXF2 protein has been recently found to be partner of FMRP in regulating Nxf1 mRNA stability in neuronal cells.]. 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:20096387
;
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:NP581379.RAYJWf36_uKWtTIksR3Xgj4KxiXm-Pij6E-7mEbxl_ans130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:50+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" .
}