@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc
> .
@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:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_head
{
this:
np:hasAssertion
dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_assertion
;
np:hasProvenance
dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_provenance
;
np:hasPublicationInfo
dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_assertion
a
np:Assertion
.
dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_provenance
a
np:Provenance
.
dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_assertion
{
miriam-gene:2481
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGNda894fec20d2c759a6f122cfc73b605a
sio:SIO_000628
miriam-gene:2481
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_provenance
{
dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_assertion
dcterms:description
"[In contrast, a relationship between the second main group of fragile sites characterized by repeat expansion, the rare fragile sites, and mental retardation has been proposed many years ago, but after the molecular cloning of FRAXA and FRAXE both unequivocally involved in mental retardation, no additional fragile sites linked with mental retardation have been cloned for over a decade.]. 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:17567780
;
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:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:26+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" .
}