@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP818199.RAYm6S-V-YbeykfmRggzHoZ33FhN8Aswfe3B0rRUfbKRA
> .
@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/v3.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP818199.RAYm6S-V-YbeykfmRggzHoZ33FhN8Aswfe3B0rRUfbKRA130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP818199.RAYm6S-V-YbeykfmRggzHoZ33FhN8Aswfe3B0rRUfbKRA130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP818199.RAYm6S-V-YbeykfmRggzHoZ33FhN8Aswfe3B0rRUfbKRA130_assertion
a
np:Assertion
.
dgn-np:NP818199.RAYm6S-V-YbeykfmRggzHoZ33FhN8Aswfe3B0rRUfbKRA130_provenance
a
np:Provenance
.
dgn-np:NP818199.RAYm6S-V-YbeykfmRggzHoZ33FhN8Aswfe3B0rRUfbKRA130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:9223
a
ncit:C16612
.
lld:C1456781
a
ncit:C7057
.
dgn-gda:DGN90f8bcf041ad0e916e46308fc3bcd21f
sio:SIO_000628
miriam-gene:9223
,
lld:C1456781
;
a
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.
}
dgn-np:NP818199.RAYm6S-V-YbeykfmRggzHoZ33FhN8Aswfe3B0rRUfbKRA130_provenance
{
dgn-np:NP818199.RAYm6S-V-YbeykfmRggzHoZ33FhN8Aswfe3B0rRUfbKRA130_assertion
dcterms:description
"[Herein are illustrated some pitfalls in the diagnosis of melanoma, as well as variants of Spitz's nevus that correlate with specific genomic aberrations such as gains of chromosome 11p and loss of the BAP-1 gene on chromosome 3p.]. 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:22648325
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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 .
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dgn-np:NP818199.RAYm6S-V-YbeykfmRggzHoZ33FhN8Aswfe3B0rRUfbKRA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:56+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
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> ;
pav:createdBy
<
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> ;
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"v3.0.0" .
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