@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP189386.RAW7Z-TYfO_Z_7IfAuZkhveMrQxuiZrsKwhvyXTiXjOKc
> .
@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:NP189386.RAW7Z-TYfO_Z_7IfAuZkhveMrQxuiZrsKwhvyXTiXjOKc130_head
{
this:
np:hasAssertion
dgn-np:NP189386.RAW7Z-TYfO_Z_7IfAuZkhveMrQxuiZrsKwhvyXTiXjOKc130_assertion
;
np:hasProvenance
dgn-np:NP189386.RAW7Z-TYfO_Z_7IfAuZkhveMrQxuiZrsKwhvyXTiXjOKc130_provenance
;
np:hasPublicationInfo
dgn-np:NP189386.RAW7Z-TYfO_Z_7IfAuZkhveMrQxuiZrsKwhvyXTiXjOKc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP189386.RAW7Z-TYfO_Z_7IfAuZkhveMrQxuiZrsKwhvyXTiXjOKc130_assertion
a
np:Assertion
.
dgn-np:NP189386.RAW7Z-TYfO_Z_7IfAuZkhveMrQxuiZrsKwhvyXTiXjOKc130_provenance
a
np:Provenance
.
dgn-np:NP189386.RAW7Z-TYfO_Z_7IfAuZkhveMrQxuiZrsKwhvyXTiXjOKc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP189386.RAW7Z-TYfO_Z_7IfAuZkhveMrQxuiZrsKwhvyXTiXjOKc130_assertion
{
miriam-gene:1033
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN5be26ffd2426d33c276a39360dc10c39
sio:SIO_000628
miriam-gene:1033
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP189386.RAW7Z-TYfO_Z_7IfAuZkhveMrQxuiZrsKwhvyXTiXjOKc130_provenance
{
dgn-np:NP189386.RAW7Z-TYfO_Z_7IfAuZkhveMrQxuiZrsKwhvyXTiXjOKc130_assertion
dcterms:description
"[Although homozygous deletions of the cyclin-dependent kinase inhibitor 2 gene p16INK4a on 9p21 have been reported frequently in metastatic melanoma cell lines, and intragenic mutations within the p16INK4a gene have been detected in familial melanoma kindreds, specific targeting of this gene in the development of sporadic melanoma in vivo remains controversial.]. 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:8895759
;
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:NP189386.RAW7Z-TYfO_Z_7IfAuZkhveMrQxuiZrsKwhvyXTiXjOKc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}