@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP787886.RA5ijbWboSN2RluKr4aXMBsHD4yTfaf5DVDf9kMpCJLgE
> .
@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:NP787886.RA5ijbWboSN2RluKr4aXMBsHD4yTfaf5DVDf9kMpCJLgE130_head
{
this:
np:hasAssertion
dgn-np:NP787886.RA5ijbWboSN2RluKr4aXMBsHD4yTfaf5DVDf9kMpCJLgE130_assertion
;
np:hasProvenance
dgn-np:NP787886.RA5ijbWboSN2RluKr4aXMBsHD4yTfaf5DVDf9kMpCJLgE130_provenance
;
np:hasPublicationInfo
dgn-np:NP787886.RA5ijbWboSN2RluKr4aXMBsHD4yTfaf5DVDf9kMpCJLgE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP787886.RA5ijbWboSN2RluKr4aXMBsHD4yTfaf5DVDf9kMpCJLgE130_assertion
a
np:Assertion
.
dgn-np:NP787886.RA5ijbWboSN2RluKr4aXMBsHD4yTfaf5DVDf9kMpCJLgE130_provenance
a
np:Provenance
.
dgn-np:NP787886.RA5ijbWboSN2RluKr4aXMBsHD4yTfaf5DVDf9kMpCJLgE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP787886.RA5ijbWboSN2RluKr4aXMBsHD4yTfaf5DVDf9kMpCJLgE130_assertion
{
miriam-gene:1030
a
ncit:C16612
.
lld:C0026948
a
ncit:C7057
.
dgn-gda:DGN65acf5ff8105c0c6af9f34b39fa20b74
sio:SIO_000628
miriam-gene:1030
,
lld:C0026948
;
a
sio:SIO_001121
.
}
dgn-np:NP787886.RA5ijbWboSN2RluKr4aXMBsHD4yTfaf5DVDf9kMpCJLgE130_provenance
{
dgn-np:NP787886.RA5ijbWboSN2RluKr4aXMBsHD4yTfaf5DVDf9kMpCJLgE130_assertion
dcterms:description
"[Because the 9p21 locus seems to be a good target for a detailed study in MF, this prompted us to compare the mechanisms of inactivation of the p16(INK4a), p15(INK4b), and p14(ARF) genes in aggressive and stable forms of MF, performing microsatellite analysis, methylation-specific polymerase chain reaction, direct sequencing, and p16(INK4a) protein expression by immunohistochemistry.]. 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:11850526
;
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:NP787886.RA5ijbWboSN2RluKr4aXMBsHD4yTfaf5DVDf9kMpCJLgE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:00+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" .
}