@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP806373.RAKF48gwymsnLrHcjFIss8LIU9gztgfEzv4mz2gHgeqVM
> .
@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:NP806373.RAKF48gwymsnLrHcjFIss8LIU9gztgfEzv4mz2gHgeqVM130_head
{
this:
np:hasAssertion
dgn-np:NP806373.RAKF48gwymsnLrHcjFIss8LIU9gztgfEzv4mz2gHgeqVM130_assertion
;
np:hasProvenance
dgn-np:NP806373.RAKF48gwymsnLrHcjFIss8LIU9gztgfEzv4mz2gHgeqVM130_provenance
;
np:hasPublicationInfo
dgn-np:NP806373.RAKF48gwymsnLrHcjFIss8LIU9gztgfEzv4mz2gHgeqVM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP806373.RAKF48gwymsnLrHcjFIss8LIU9gztgfEzv4mz2gHgeqVM130_assertion
a
np:Assertion
.
dgn-np:NP806373.RAKF48gwymsnLrHcjFIss8LIU9gztgfEzv4mz2gHgeqVM130_provenance
a
np:Provenance
.
dgn-np:NP806373.RAKF48gwymsnLrHcjFIss8LIU9gztgfEzv4mz2gHgeqVM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP806373.RAKF48gwymsnLrHcjFIss8LIU9gztgfEzv4mz2gHgeqVM130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0042769
a
ncit:C7057
.
dgn-gda:DGNb8fd1c04ff23ddeb9a7791798873f7b2
sio:SIO_000628
miriam-gene:3630
,
lld:C0042769
;
a
sio:SIO_001121
.
}
dgn-np:NP806373.RAKF48gwymsnLrHcjFIss8LIU9gztgfEzv4mz2gHgeqVM130_provenance
{
dgn-np:NP806373.RAKF48gwymsnLrHcjFIss8LIU9gztgfEzv4mz2gHgeqVM130_assertion
dcterms:description
"[They have been implicated in the regulation of developmental timing and pattern formation, restriction of differentiation potential, regulation of insulin secretion, resistance to viral infection, and in genomic rearrangements associated with carcinogenesis or other genetic disorders, such as 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:17402793
;
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:NP806373.RAKF48gwymsnLrHcjFIss8LIU9gztgfEzv4mz2gHgeqVM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:14+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" .
}