@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP500419.RA316sNGqqrCSnjqBNxlpN6ExL8S6sY4wqpjI0dZ0c450
> .
@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:NP500419.RA316sNGqqrCSnjqBNxlpN6ExL8S6sY4wqpjI0dZ0c450130_head
{
this:
np:hasAssertion
dgn-np:NP500419.RA316sNGqqrCSnjqBNxlpN6ExL8S6sY4wqpjI0dZ0c450130_assertion
;
np:hasProvenance
dgn-np:NP500419.RA316sNGqqrCSnjqBNxlpN6ExL8S6sY4wqpjI0dZ0c450130_provenance
;
np:hasPublicationInfo
dgn-np:NP500419.RA316sNGqqrCSnjqBNxlpN6ExL8S6sY4wqpjI0dZ0c450130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP500419.RA316sNGqqrCSnjqBNxlpN6ExL8S6sY4wqpjI0dZ0c450130_assertion
a
np:Assertion
.
dgn-np:NP500419.RA316sNGqqrCSnjqBNxlpN6ExL8S6sY4wqpjI0dZ0c450130_provenance
a
np:Provenance
.
dgn-np:NP500419.RA316sNGqqrCSnjqBNxlpN6ExL8S6sY4wqpjI0dZ0c450130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP500419.RA316sNGqqrCSnjqBNxlpN6ExL8S6sY4wqpjI0dZ0c450130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0006118
a
ncit:C7057
.
dgn-gda:DGN116f967a9c7648b211f34cc47cc7e162
sio:SIO_000628
miriam-gene:1029
,
lld:C0006118
;
a
sio:SIO_001121
.
}
dgn-np:NP500419.RA316sNGqqrCSnjqBNxlpN6ExL8S6sY4wqpjI0dZ0c450130_provenance
{
dgn-np:NP500419.RA316sNGqqrCSnjqBNxlpN6ExL8S6sY4wqpjI0dZ0c450130_assertion
dcterms:description
"[The frequency of the alteration of the p16 gene, either homozygous deletion or mutation accompanied with amino acid substitutions, increased in malignant brain tumors (grade III and IV) compared with that in low grade tumors (grade I and II) (p=0.0275), suggesting possible role(s) of the gene in the progression of brain tumors.]. 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:10536183
;
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:NP500419.RA316sNGqqrCSnjqBNxlpN6ExL8S6sY4wqpjI0dZ0c450130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+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" .
}