@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1355247.RAusGa1VKw8Jz2ymLA3svSKfECl69pyz20NxnNG0OkGTg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1355247.RAusGa1VKw8Jz2ymLA3svSKfECl69pyz20NxnNG0OkGTg130_head
{
this:
np:hasAssertion
dgn-np:NP1355247.RAusGa1VKw8Jz2ymLA3svSKfECl69pyz20NxnNG0OkGTg130_assertion
;
np:hasProvenance
dgn-np:NP1355247.RAusGa1VKw8Jz2ymLA3svSKfECl69pyz20NxnNG0OkGTg130_provenance
;
np:hasPublicationInfo
dgn-np:NP1355247.RAusGa1VKw8Jz2ymLA3svSKfECl69pyz20NxnNG0OkGTg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1355247.RAusGa1VKw8Jz2ymLA3svSKfECl69pyz20NxnNG0OkGTg130_assertion
a
np:Assertion
.
dgn-np:NP1355247.RAusGa1VKw8Jz2ymLA3svSKfECl69pyz20NxnNG0OkGTg130_provenance
a
np:Provenance
.
dgn-np:NP1355247.RAusGa1VKw8Jz2ymLA3svSKfECl69pyz20NxnNG0OkGTg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1355247.RAusGa1VKw8Jz2ymLA3svSKfECl69pyz20NxnNG0OkGTg130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0151779
a
ncit:C7057
.
dgn-gda:DGN0263c150cb412cc69f9fa9dc1778cd63
sio:SIO_000628
miriam-gene:1029
,
lld:C0151779
;
a
sio:SIO_001121
.
}
dgn-np:NP1355247.RAusGa1VKw8Jz2ymLA3svSKfECl69pyz20NxnNG0OkGTg130_provenance
{
dgn-np:NP1355247.RAusGa1VKw8Jz2ymLA3svSKfECl69pyz20NxnNG0OkGTg130_assertion
dcterms:description
"[The inactivation of both copies of p16INK4 in the one case of melanoma adds support to the theory that p16INK4 is important in the development of sporadic cutaneous melanoma, although allelic loss or other methods of inactivation of p16INK4 rather than point mutation appears to be numerically more important.]. 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:8751963
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1355247.RAusGa1VKw8Jz2ymLA3svSKfECl69pyz20NxnNG0OkGTg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:00+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}