@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP279582.RAUk49DZaF5eJSXSM22kJBpCMMg9zmEGuGHGm64lFmMzI
> .
@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:NP279582.RAUk49DZaF5eJSXSM22kJBpCMMg9zmEGuGHGm64lFmMzI130_head
{
this:
np:hasAssertion
dgn-np:NP279582.RAUk49DZaF5eJSXSM22kJBpCMMg9zmEGuGHGm64lFmMzI130_assertion
;
np:hasProvenance
dgn-np:NP279582.RAUk49DZaF5eJSXSM22kJBpCMMg9zmEGuGHGm64lFmMzI130_provenance
;
np:hasPublicationInfo
dgn-np:NP279582.RAUk49DZaF5eJSXSM22kJBpCMMg9zmEGuGHGm64lFmMzI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP279582.RAUk49DZaF5eJSXSM22kJBpCMMg9zmEGuGHGm64lFmMzI130_assertion
a
np:Assertion
.
dgn-np:NP279582.RAUk49DZaF5eJSXSM22kJBpCMMg9zmEGuGHGm64lFmMzI130_provenance
a
np:Provenance
.
dgn-np:NP279582.RAUk49DZaF5eJSXSM22kJBpCMMg9zmEGuGHGm64lFmMzI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP279582.RAUk49DZaF5eJSXSM22kJBpCMMg9zmEGuGHGm64lFmMzI130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0027766
a
ncit:C7057
.
dgn-gda:DGN3f30b9fce54ffa1578a65dfc1c1d4e0f
sio:SIO_000628
miriam-gene:1029
,
lld:C0027766
;
a
sio:SIO_001121
.
}
dgn-np:NP279582.RAUk49DZaF5eJSXSM22kJBpCMMg9zmEGuGHGm64lFmMzI130_provenance
{
dgn-np:NP279582.RAUk49DZaF5eJSXSM22kJBpCMMg9zmEGuGHGm64lFmMzI130_assertion
dcterms:description
"[Although the group of patients was heterogeneous, our results are in accordance with other different studies that indicate that homozygous deletion and loss of heterozygosity in the INK4 family members are frequently observed in nervous system 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:18551412
;
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:NP279582.RAUk49DZaF5eJSXSM22kJBpCMMg9zmEGuGHGm64lFmMzI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+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" .
}