@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP756979.RAXI0z2ghwybZVgUYDbOLFZoiBu7wmLemglU_Aro6H9Sg
> .
@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:NP756979.RAXI0z2ghwybZVgUYDbOLFZoiBu7wmLemglU_Aro6H9Sg130_head
{
this:
np:hasAssertion
dgn-np:NP756979.RAXI0z2ghwybZVgUYDbOLFZoiBu7wmLemglU_Aro6H9Sg130_assertion
;
np:hasProvenance
dgn-np:NP756979.RAXI0z2ghwybZVgUYDbOLFZoiBu7wmLemglU_Aro6H9Sg130_provenance
;
np:hasPublicationInfo
dgn-np:NP756979.RAXI0z2ghwybZVgUYDbOLFZoiBu7wmLemglU_Aro6H9Sg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP756979.RAXI0z2ghwybZVgUYDbOLFZoiBu7wmLemglU_Aro6H9Sg130_assertion
a
np:Assertion
.
dgn-np:NP756979.RAXI0z2ghwybZVgUYDbOLFZoiBu7wmLemglU_Aro6H9Sg130_provenance
a
np:Provenance
.
dgn-np:NP756979.RAXI0z2ghwybZVgUYDbOLFZoiBu7wmLemglU_Aro6H9Sg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP756979.RAXI0z2ghwybZVgUYDbOLFZoiBu7wmLemglU_Aro6H9Sg130_assertion
{
miriam-gene:6275
a
ncit:C16612
.
lld:C0004114
a
ncit:C7057
.
dgn-gda:DGN7077062a8c4eb51eaf6b7266f005a9d0
sio:SIO_000628
miriam-gene:6275
,
lld:C0004114
;
a
sio:SIO_001121
.
}
dgn-np:NP756979.RAXI0z2ghwybZVgUYDbOLFZoiBu7wmLemglU_Aro6H9Sg130_provenance
{
dgn-np:NP756979.RAXI0z2ghwybZVgUYDbOLFZoiBu7wmLemglU_Aro6H9Sg130_assertion
dcterms:description
"[The low frequency of MTS1 mutations in primary astrocytomas with allelic 9p loss suggests that MTS1 may be more important for in vitro than in vivo astrocytoma growth, and that another 9p tumor suppressor gene may be involved in astrocytoma formation in vivo.]. 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:7849711
;
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:NP756979.RAXI0z2ghwybZVgUYDbOLFZoiBu7wmLemglU_Aro6H9Sg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:38+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" .
}