@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg
> .
@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:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_head
{
this:
np:hasAssertion
dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_assertion
;
np:hasProvenance
dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_provenance
;
np:hasPublicationInfo
dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_assertion
a
np:Assertion
.
dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_provenance
a
np:Provenance
.
dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_assertion
{
miriam-gene:2521
a
ncit:C16612
.
lld:C0016412
a
ncit:C7057
.
dgn-gda:DGNf5456e21031a6eaea18a26ec4b30f322
sio:SIO_000628
miriam-gene:2521
,
lld:C0016412
;
a
sio:SIO_001121
.
}
dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_provenance
{
dgn-np:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_assertion
dcterms:description
"[It was concluded that the FUS, CIR, and HS morphologies represent promising biomarkers of CIN that are sensitive to folate deficiency, and further validation and investigation of the mechanisms responsible for their formation is warranted.]. 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:22430981
;
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:NP493741.RAaQc8Mt2f1QWW4A9HFK0e1LfLDQ49E0qqlak0mx0UmAg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:55+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" .
}