@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4
> .
@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:NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_head
{
this:
np:hasAssertion
dgn-np:NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_assertion
;
np:hasProvenance
dgn-np:NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_provenance
;
np:hasPublicationInfo
dgn-np:NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_assertion
a
np:Assertion
.
dgn-np:NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_provenance
a
np:Provenance
.
dgn-np:NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0346040
a
ncit:C7057
.
dgn-gda:DGN4acb28e1a4afb1c73a09d2ed5350cf47
sio:SIO_000628
miriam-gene:1029
,
lld:C0346040
;
a
sio:SIO_001121
.
}
dgn-np:NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_provenance
{
dgn-np:NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_assertion
dcterms:description
"[Among many gene alterations detected in human melanoma, defect of CDKN2A located at chromosome 9p21 seems to be most important in the earlier developmental phase, though significance of this gene in the evolution of melanoma in situ has not been confirmed yet.]. 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:11323215
;
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:NP664016.RADfzqn3xR-AUc_9fUodCgRv2tySyVVNdFJ3QVY56AdD4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:41+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" .
}