@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP918264.RAZMvP-LE083YUBi0702Sf_RYE_PMDWW3NOXh_fuqKmfk
> .
@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:NP918264.RAZMvP-LE083YUBi0702Sf_RYE_PMDWW3NOXh_fuqKmfk130_head
{
this:
np:hasAssertion
dgn-np:NP918264.RAZMvP-LE083YUBi0702Sf_RYE_PMDWW3NOXh_fuqKmfk130_assertion
;
np:hasProvenance
dgn-np:NP918264.RAZMvP-LE083YUBi0702Sf_RYE_PMDWW3NOXh_fuqKmfk130_provenance
;
np:hasPublicationInfo
dgn-np:NP918264.RAZMvP-LE083YUBi0702Sf_RYE_PMDWW3NOXh_fuqKmfk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP918264.RAZMvP-LE083YUBi0702Sf_RYE_PMDWW3NOXh_fuqKmfk130_assertion
a
np:Assertion
.
dgn-np:NP918264.RAZMvP-LE083YUBi0702Sf_RYE_PMDWW3NOXh_fuqKmfk130_provenance
a
np:Provenance
.
dgn-np:NP918264.RAZMvP-LE083YUBi0702Sf_RYE_PMDWW3NOXh_fuqKmfk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP918264.RAZMvP-LE083YUBi0702Sf_RYE_PMDWW3NOXh_fuqKmfk130_assertion
{
miriam-gene:3125
a
ncit:C16612
.
lld:C0334444
a
ncit:C7057
.
dgn-gda:DGN94a73297add99041463571340abc271e
sio:SIO_000628
miriam-gene:3125
,
lld:C0334444
;
a
sio:SIO_001121
.
}
dgn-np:NP918264.RAZMvP-LE083YUBi0702Sf_RYE_PMDWW3NOXh_fuqKmfk130_provenance
{
dgn-np:NP918264.RAZMvP-LE083YUBi0702Sf_RYE_PMDWW3NOXh_fuqKmfk130_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:NP918264.RAZMvP-LE083YUBi0702Sf_RYE_PMDWW3NOXh_fuqKmfk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:23+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" .
}