@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP257435.RAHZP4XQuV7-6eCGuCdpcAohLaIiLkX53yIatwrmbM6zE
> .
@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:NP257435.RAHZP4XQuV7-6eCGuCdpcAohLaIiLkX53yIatwrmbM6zE130_head
{
this:
np:hasAssertion
dgn-np:NP257435.RAHZP4XQuV7-6eCGuCdpcAohLaIiLkX53yIatwrmbM6zE130_assertion
;
np:hasProvenance
dgn-np:NP257435.RAHZP4XQuV7-6eCGuCdpcAohLaIiLkX53yIatwrmbM6zE130_provenance
;
np:hasPublicationInfo
dgn-np:NP257435.RAHZP4XQuV7-6eCGuCdpcAohLaIiLkX53yIatwrmbM6zE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP257435.RAHZP4XQuV7-6eCGuCdpcAohLaIiLkX53yIatwrmbM6zE130_assertion
a
np:Assertion
.
dgn-np:NP257435.RAHZP4XQuV7-6eCGuCdpcAohLaIiLkX53yIatwrmbM6zE130_provenance
a
np:Provenance
.
dgn-np:NP257435.RAHZP4XQuV7-6eCGuCdpcAohLaIiLkX53yIatwrmbM6zE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP257435.RAHZP4XQuV7-6eCGuCdpcAohLaIiLkX53yIatwrmbM6zE130_assertion
{
miriam-gene:4763
a
ncit:C16612
.
lld:C0346326
a
ncit:C7057
.
dgn-gda:DGN2083d181fe984b403092f33e0b692915
sio:SIO_000628
miriam-gene:4763
,
lld:C0346326
;
a
sio:SIO_001121
.
}
dgn-np:NP257435.RAHZP4XQuV7-6eCGuCdpcAohLaIiLkX53yIatwrmbM6zE130_provenance
{
dgn-np:NP257435.RAHZP4XQuV7-6eCGuCdpcAohLaIiLkX53yIatwrmbM6zE130_assertion
dcterms:description
"[Our results present the clustering of mutations in the 5'tertile of NF1 gene in patients with optic nerve glioma and suggest higher incidence of freckling and neurofibromatosis brain objects in these patients.]. 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:23906300
;
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:NP257435.RAHZP4XQuV7-6eCGuCdpcAohLaIiLkX53yIatwrmbM6zE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:24+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" .
}