@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP979486.RAiPBHrLYrhRkN3j2SI7gKZhJXpPTiMwjBTs3h0QafxMY
> .
@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/v4.0.0/void/
> .
dgn-np:NP979486.RAiPBHrLYrhRkN3j2SI7gKZhJXpPTiMwjBTs3h0QafxMY130_head
{
this:
np:hasAssertion
dgn-np:NP979486.RAiPBHrLYrhRkN3j2SI7gKZhJXpPTiMwjBTs3h0QafxMY130_assertion
;
np:hasProvenance
dgn-np:NP979486.RAiPBHrLYrhRkN3j2SI7gKZhJXpPTiMwjBTs3h0QafxMY130_provenance
;
np:hasPublicationInfo
dgn-np:NP979486.RAiPBHrLYrhRkN3j2SI7gKZhJXpPTiMwjBTs3h0QafxMY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP979486.RAiPBHrLYrhRkN3j2SI7gKZhJXpPTiMwjBTs3h0QafxMY130_assertion
a
np:Assertion
.
dgn-np:NP979486.RAiPBHrLYrhRkN3j2SI7gKZhJXpPTiMwjBTs3h0QafxMY130_provenance
a
np:Provenance
.
dgn-np:NP979486.RAiPBHrLYrhRkN3j2SI7gKZhJXpPTiMwjBTs3h0QafxMY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP979486.RAiPBHrLYrhRkN3j2SI7gKZhJXpPTiMwjBTs3h0QafxMY130_assertion
{
miriam-gene:4286
a
ncit:C16612
.
lld:C0206735
a
ncit:C7057
.
dgn-gda:DGNfcfd31dd7203bc025c5b19fa2b1d1d3e
sio:SIO_000628
miriam-gene:4286
,
lld:C0206735
;
a
sio:SIO_001121
.
}
dgn-np:NP979486.RAiPBHrLYrhRkN3j2SI7gKZhJXpPTiMwjBTs3h0QafxMY130_provenance
{
dgn-np:NP979486.RAiPBHrLYrhRkN3j2SI7gKZhJXpPTiMwjBTs3h0QafxMY130_assertion
dcterms:description
"[As MITF is a frequently used marker to establish melanocytic lineage in melanoma, our study also raises the important clinical consideration that amelanotic melanomas, especially those with gains in 8q24 may lack expression of MITF.]. 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:22555175
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP979486.RAiPBHrLYrhRkN3j2SI7gKZhJXpPTiMwjBTs3h0QafxMY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:08+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}