@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP549003.RARwAFc98ozvJKyi2ek0qNinJ783riy1YYRWXQd-Ou0so
> .
@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:NP549003.RARwAFc98ozvJKyi2ek0qNinJ783riy1YYRWXQd-Ou0so130_head
{
this:
np:hasAssertion
dgn-np:NP549003.RARwAFc98ozvJKyi2ek0qNinJ783riy1YYRWXQd-Ou0so130_assertion
;
np:hasProvenance
dgn-np:NP549003.RARwAFc98ozvJKyi2ek0qNinJ783riy1YYRWXQd-Ou0so130_provenance
;
np:hasPublicationInfo
dgn-np:NP549003.RARwAFc98ozvJKyi2ek0qNinJ783riy1YYRWXQd-Ou0so130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP549003.RARwAFc98ozvJKyi2ek0qNinJ783riy1YYRWXQd-Ou0so130_assertion
a
np:Assertion
.
dgn-np:NP549003.RARwAFc98ozvJKyi2ek0qNinJ783riy1YYRWXQd-Ou0so130_provenance
a
np:Provenance
.
dgn-np:NP549003.RARwAFc98ozvJKyi2ek0qNinJ783riy1YYRWXQd-Ou0so130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP549003.RARwAFc98ozvJKyi2ek0qNinJ783riy1YYRWXQd-Ou0so130_assertion
{
miriam-gene:56247
a
ncit:C16612
.
lld:C0006009
a
ncit:C7057
.
dgn-gda:DGN5af606ce1b6333b0d21f0fce1cd9f0bb
sio:SIO_000628
miriam-gene:56247
,
lld:C0006009
;
a
sio:SIO_001121
.
}
dgn-np:NP549003.RARwAFc98ozvJKyi2ek0qNinJ783riy1YYRWXQd-Ou0so130_provenance
{
dgn-np:NP549003.RARwAFc98ozvJKyi2ek0qNinJ783riy1YYRWXQd-Ou0so130_assertion
dcterms:description
"[Although the role of FMR3 in FRAXE associated mild to borderline mental retardation is not yet clear, lack of expression of FMR3 in FRAXE full mutation males means that the FMR3 gene is potentially involved.]. 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:11015457
;
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:NP549003.RARwAFc98ozvJKyi2ek0qNinJ783riy1YYRWXQd-Ou0so130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:31+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" .
}