@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP388377.RAOOj1qzS5y4jYExbG8r8aac87YwXnomg7cFm9GELhaSo
> .
@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:NP388377.RAOOj1qzS5y4jYExbG8r8aac87YwXnomg7cFm9GELhaSo130_head
{
this:
np:hasAssertion
dgn-np:NP388377.RAOOj1qzS5y4jYExbG8r8aac87YwXnomg7cFm9GELhaSo130_assertion
;
np:hasProvenance
dgn-np:NP388377.RAOOj1qzS5y4jYExbG8r8aac87YwXnomg7cFm9GELhaSo130_provenance
;
np:hasPublicationInfo
dgn-np:NP388377.RAOOj1qzS5y4jYExbG8r8aac87YwXnomg7cFm9GELhaSo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP388377.RAOOj1qzS5y4jYExbG8r8aac87YwXnomg7cFm9GELhaSo130_assertion
a
np:Assertion
.
dgn-np:NP388377.RAOOj1qzS5y4jYExbG8r8aac87YwXnomg7cFm9GELhaSo130_provenance
a
np:Provenance
.
dgn-np:NP388377.RAOOj1qzS5y4jYExbG8r8aac87YwXnomg7cFm9GELhaSo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP388377.RAOOj1qzS5y4jYExbG8r8aac87YwXnomg7cFm9GELhaSo130_assertion
{
miriam-gene:8502
a
ncit:C16612
.
lld:C0016667
a
ncit:C7057
.
dgn-gda:DGNb91eb79c16899caed5ed255292d765a2
sio:SIO_000628
miriam-gene:8502
,
lld:C0016667
;
a
sio:SIO_001121
.
}
dgn-np:NP388377.RAOOj1qzS5y4jYExbG8r8aac87YwXnomg7cFm9GELhaSo130_provenance
{
dgn-np:NP388377.RAOOj1qzS5y4jYExbG8r8aac87YwXnomg7cFm9GELhaSo130_assertion
dcterms:description
"[These results identify p0071 as an important and novel FMRP target and strongly suggest that impaired actin cytoskeletal functions mediated by an excess of p0071 are key aspects underlying the fragile X syndrome.]. 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:24062571
;
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:NP388377.RAOOj1qzS5y4jYExbG8r8aac87YwXnomg7cFm9GELhaSo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:51+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" .
}