@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP864828.RA_PHllt8U_YIXaLxsTJgdNjv4ORSdBASg8xDqLNcKWbs
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP864828.RA_PHllt8U_YIXaLxsTJgdNjv4ORSdBASg8xDqLNcKWbs130_assertion
;
np:hasProvenance
dgn-np:NP864828.RA_PHllt8U_YIXaLxsTJgdNjv4ORSdBASg8xDqLNcKWbs130_provenance
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np:hasPublicationInfo
dgn-np:NP864828.RA_PHllt8U_YIXaLxsTJgdNjv4ORSdBASg8xDqLNcKWbs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP864828.RA_PHllt8U_YIXaLxsTJgdNjv4ORSdBASg8xDqLNcKWbs130_assertion
a
np:Assertion
.
dgn-np:NP864828.RA_PHllt8U_YIXaLxsTJgdNjv4ORSdBASg8xDqLNcKWbs130_provenance
a
np:Provenance
.
dgn-np:NP864828.RA_PHllt8U_YIXaLxsTJgdNjv4ORSdBASg8xDqLNcKWbs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP864828.RA_PHllt8U_YIXaLxsTJgdNjv4ORSdBASg8xDqLNcKWbs130_assertion
{
miriam-gene:5573
a
ncit:C16612
.
lld:C0334431
a
ncit:C7057
.
dgn-gda:DGN073aaa6d01e2d4f4cde6e12190455335
sio:SIO_000628
miriam-gene:5573
,
lld:C0334431
;
a
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.
}
dgn-np:NP864828.RA_PHllt8U_YIXaLxsTJgdNjv4ORSdBASg8xDqLNcKWbs130_provenance
{
dgn-np:NP864828.RA_PHllt8U_YIXaLxsTJgdNjv4ORSdBASg8xDqLNcKWbs130_assertion
dcterms:description
"[In this study, we investigated whether PEM and EBN are related at the molecular level, and whether changes in the PRKAR1A gene status and the expression of the R1alpha protein may be involved in the pathogenesis of PEM and other melanocytic lesions.]. 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:18059235
;
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 .
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dgn-np:NP864828.RA_PHllt8U_YIXaLxsTJgdNjv4ORSdBASg8xDqLNcKWbs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:48+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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