@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP699159.RASnXE0fd_K7FeCg5cL7Wu1kFwFGyheAGWWl0AtmExoac
> .
@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:NP699159.RASnXE0fd_K7FeCg5cL7Wu1kFwFGyheAGWWl0AtmExoac130_head
{
this:
np:hasAssertion
dgn-np:NP699159.RASnXE0fd_K7FeCg5cL7Wu1kFwFGyheAGWWl0AtmExoac130_assertion
;
np:hasProvenance
dgn-np:NP699159.RASnXE0fd_K7FeCg5cL7Wu1kFwFGyheAGWWl0AtmExoac130_provenance
;
np:hasPublicationInfo
dgn-np:NP699159.RASnXE0fd_K7FeCg5cL7Wu1kFwFGyheAGWWl0AtmExoac130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP699159.RASnXE0fd_K7FeCg5cL7Wu1kFwFGyheAGWWl0AtmExoac130_assertion
a
np:Assertion
.
dgn-np:NP699159.RASnXE0fd_K7FeCg5cL7Wu1kFwFGyheAGWWl0AtmExoac130_provenance
a
np:Provenance
.
dgn-np:NP699159.RASnXE0fd_K7FeCg5cL7Wu1kFwFGyheAGWWl0AtmExoac130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP699159.RASnXE0fd_K7FeCg5cL7Wu1kFwFGyheAGWWl0AtmExoac130_assertion
{
miriam-gene:3125
a
ncit:C16612
.
lld:C0220633
a
ncit:C7057
.
dgn-gda:DGNe9141bd91b5b519b9b9f86d287e9b220
sio:SIO_000628
miriam-gene:3125
,
lld:C0220633
;
a
sio:SIO_001121
.
}
dgn-np:NP699159.RASnXE0fd_K7FeCg5cL7Wu1kFwFGyheAGWWl0AtmExoac130_provenance
{
dgn-np:NP699159.RASnXE0fd_K7FeCg5cL7Wu1kFwFGyheAGWWl0AtmExoac130_assertion
dcterms:description
"[The deviated frequencies of class I HLA antigens (A32, B27) seem to be involved in the predisposition to spindle cell melanoma, while HLA class II (DR3, DR7) and class III (Bf F) strongly mark the worst form of UM.]. 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:3180122
;
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:NP699159.RASnXE0fd_K7FeCg5cL7Wu1kFwFGyheAGWWl0AtmExoac130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:05+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" .
}