@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc
> .
@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:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_head
{
this:
np:hasAssertion
dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_assertion
;
np:hasProvenance
dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_provenance
;
np:hasPublicationInfo
dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_assertion
a
np:Assertion
.
dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_provenance
a
np:Provenance
.
dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_assertion
{
miriam-gene:768
a
ncit:C16612
.
lld:C0334424
a
ncit:C7057
.
dgn-gda:DGN380312019287fe60fc0776d45d18f82b
sio:SIO_000628
miriam-gene:768
,
lld:C0334424
;
a
sio:SIO_001121
.
}
dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_provenance
{
dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_assertion
dcterms:description
"[A well characterized series of nodular melanoma (originally 202 cases) and other benign and malignant melanocytic tumors (109 cases) were examined for the presence of necrosis, apoptotic activity (TUNEL assay), immunohistochemical expression of hypoxia markers (HIF-1 alpha, CAIX, TNF-alpha, Apaf-1) and cell adhesion proteins (alphavbeta3 integrin, CD44/HCAM and osteopontin).]. 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:19061491
;
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:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:52+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" .
}