@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP130692.RAGfuvLV1kILjjzm51iLgSMk-CEPP3CRwz0kH6af2krwc
> .
@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:NP130692.RAGfuvLV1kILjjzm51iLgSMk-CEPP3CRwz0kH6af2krwc130_head
{
this:
np:hasAssertion
dgn-np:NP130692.RAGfuvLV1kILjjzm51iLgSMk-CEPP3CRwz0kH6af2krwc130_assertion
;
np:hasProvenance
dgn-np:NP130692.RAGfuvLV1kILjjzm51iLgSMk-CEPP3CRwz0kH6af2krwc130_provenance
;
np:hasPublicationInfo
dgn-np:NP130692.RAGfuvLV1kILjjzm51iLgSMk-CEPP3CRwz0kH6af2krwc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP130692.RAGfuvLV1kILjjzm51iLgSMk-CEPP3CRwz0kH6af2krwc130_assertion
a
np:Assertion
.
dgn-np:NP130692.RAGfuvLV1kILjjzm51iLgSMk-CEPP3CRwz0kH6af2krwc130_provenance
a
np:Provenance
.
dgn-np:NP130692.RAGfuvLV1kILjjzm51iLgSMk-CEPP3CRwz0kH6af2krwc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP130692.RAGfuvLV1kILjjzm51iLgSMk-CEPP3CRwz0kH6af2krwc130_assertion
{
miriam-gene:2332
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN4ae8c19f9d3a81b57dd06249bc8a4424
sio:SIO_000628
miriam-gene:2332
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP130692.RAGfuvLV1kILjjzm51iLgSMk-CEPP3CRwz0kH6af2krwc130_provenance
{
dgn-np:NP130692.RAGfuvLV1kILjjzm51iLgSMk-CEPP3CRwz0kH6af2krwc130_assertion
dcterms:description
"[Broad screening for premutation alleles in Parkinson disease populations is unlikely to be productive in the absence of additional clinical or family history data that suggest involvement of the FMR1 gene.]. 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:17620491
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP130692.RAGfuvLV1kILjjzm51iLgSMk-CEPP3CRwz0kH6af2krwc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:08+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" .
}