@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP497359.RA0daYS2uXc7bGVWieCk3CVNjv7wUqYwxJCpxLCtRyZEc
> .
@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:NP497359.RA0daYS2uXc7bGVWieCk3CVNjv7wUqYwxJCpxLCtRyZEc130_head
{
this:
np:hasAssertion
dgn-np:NP497359.RA0daYS2uXc7bGVWieCk3CVNjv7wUqYwxJCpxLCtRyZEc130_assertion
;
np:hasProvenance
dgn-np:NP497359.RA0daYS2uXc7bGVWieCk3CVNjv7wUqYwxJCpxLCtRyZEc130_provenance
;
np:hasPublicationInfo
dgn-np:NP497359.RA0daYS2uXc7bGVWieCk3CVNjv7wUqYwxJCpxLCtRyZEc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP497359.RA0daYS2uXc7bGVWieCk3CVNjv7wUqYwxJCpxLCtRyZEc130_assertion
a
np:Assertion
.
dgn-np:NP497359.RA0daYS2uXc7bGVWieCk3CVNjv7wUqYwxJCpxLCtRyZEc130_provenance
a
np:Provenance
.
dgn-np:NP497359.RA0daYS2uXc7bGVWieCk3CVNjv7wUqYwxJCpxLCtRyZEc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP497359.RA0daYS2uXc7bGVWieCk3CVNjv7wUqYwxJCpxLCtRyZEc130_assertion
{
miriam-gene:7389
a
ncit:C16612
.
lld:C0206656
a
ncit:C7057
.
dgn-gda:DGNc7a0243c732abde5b5ec0cbab444b94d
sio:SIO_000628
miriam-gene:7389
,
lld:C0206656
;
a
sio:SIO_001121
.
}
dgn-np:NP497359.RA0daYS2uXc7bGVWieCk3CVNjv7wUqYwxJCpxLCtRyZEc130_provenance
{
dgn-np:NP497359.RA0daYS2uXc7bGVWieCk3CVNjv7wUqYwxJCpxLCtRyZEc130_assertion
dcterms:description
"[These data implicate that in sporadic ERMS, UPD at 11p15.5 is not driven by HRAS mutations and that imbalances at 11p15.5 and HRAS mutations represent independent but cooperating events during ERMS development.]. 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:17164262
;
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:NP497359.RA0daYS2uXc7bGVWieCk3CVNjv7wUqYwxJCpxLCtRyZEc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:56+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" .
}