@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP892317.RAAXoJFzChvh5h9WSmiVgkXwNJf_aHdTMRaqNEXqDXTJg
> .
@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:NP892317.RAAXoJFzChvh5h9WSmiVgkXwNJf_aHdTMRaqNEXqDXTJg130_head
{
this:
np:hasAssertion
dgn-np:NP892317.RAAXoJFzChvh5h9WSmiVgkXwNJf_aHdTMRaqNEXqDXTJg130_assertion
;
np:hasProvenance
dgn-np:NP892317.RAAXoJFzChvh5h9WSmiVgkXwNJf_aHdTMRaqNEXqDXTJg130_provenance
;
np:hasPublicationInfo
dgn-np:NP892317.RAAXoJFzChvh5h9WSmiVgkXwNJf_aHdTMRaqNEXqDXTJg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP892317.RAAXoJFzChvh5h9WSmiVgkXwNJf_aHdTMRaqNEXqDXTJg130_assertion
a
np:Assertion
.
dgn-np:NP892317.RAAXoJFzChvh5h9WSmiVgkXwNJf_aHdTMRaqNEXqDXTJg130_provenance
a
np:Provenance
.
dgn-np:NP892317.RAAXoJFzChvh5h9WSmiVgkXwNJf_aHdTMRaqNEXqDXTJg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP892317.RAAXoJFzChvh5h9WSmiVgkXwNJf_aHdTMRaqNEXqDXTJg130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN2ca25f84410b75b5bd880552c8e2a4bd
sio:SIO_000628
miriam-gene:1029
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP892317.RAAXoJFzChvh5h9WSmiVgkXwNJf_aHdTMRaqNEXqDXTJg130_provenance
{
dgn-np:NP892317.RAAXoJFzChvh5h9WSmiVgkXwNJf_aHdTMRaqNEXqDXTJg130_assertion
dcterms:description
"[All the childhood melanoma cases were associated with loss of p16 without any correlation with their Breslow thickness whereas all the Spitz nevi and benign melanocytic nevi had strong positive nuclear and cytoplasmic expression of p16 staining.]. 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:21550132
;
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:NP892317.RAAXoJFzChvh5h9WSmiVgkXwNJf_aHdTMRaqNEXqDXTJg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:28+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" .
}