@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP162352.RAtgEJuoSE7m9WAiXPG8CEzf99QZ2ybQJMYv_M8vuxEys
> .
@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:NP162352.RAtgEJuoSE7m9WAiXPG8CEzf99QZ2ybQJMYv_M8vuxEys130_head
{
this:
np:hasAssertion
dgn-np:NP162352.RAtgEJuoSE7m9WAiXPG8CEzf99QZ2ybQJMYv_M8vuxEys130_assertion
;
np:hasProvenance
dgn-np:NP162352.RAtgEJuoSE7m9WAiXPG8CEzf99QZ2ybQJMYv_M8vuxEys130_provenance
;
np:hasPublicationInfo
dgn-np:NP162352.RAtgEJuoSE7m9WAiXPG8CEzf99QZ2ybQJMYv_M8vuxEys130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP162352.RAtgEJuoSE7m9WAiXPG8CEzf99QZ2ybQJMYv_M8vuxEys130_assertion
a
np:Assertion
.
dgn-np:NP162352.RAtgEJuoSE7m9WAiXPG8CEzf99QZ2ybQJMYv_M8vuxEys130_provenance
a
np:Provenance
.
dgn-np:NP162352.RAtgEJuoSE7m9WAiXPG8CEzf99QZ2ybQJMYv_M8vuxEys130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP162352.RAtgEJuoSE7m9WAiXPG8CEzf99QZ2ybQJMYv_M8vuxEys130_assertion
{
miriam-gene:4763
a
ncit:C16612
.
lld:C0027830
a
ncit:C7057
.
dgn-gda:DGN1751e4253cbe000bd1afc4930669cf70
sio:SIO_000628
miriam-gene:4763
,
lld:C0027830
;
a
sio:SIO_001121
.
}
dgn-np:NP162352.RAtgEJuoSE7m9WAiXPG8CEzf99QZ2ybQJMYv_M8vuxEys130_provenance
{
dgn-np:NP162352.RAtgEJuoSE7m9WAiXPG8CEzf99QZ2ybQJMYv_M8vuxEys130_assertion
dcterms:description
"[The surprisingly high frequency of microsatellite alterations suggests that the NF1 gene or another gene(s) contributing to the pathogenesis of neurofibromas might be directly or indirectly implicated in the control of genomic integrity.]. 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:7585653
;
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:NP162352.RAtgEJuoSE7m9WAiXPG8CEzf99QZ2ybQJMYv_M8vuxEys130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:28+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" .
}