@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP76817.RA5DE_20TtxcMzOkUypFgfwEugF0LGZ3iPuHTeCzf49pY
> .
@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/v3.0.0/void/
> .
dgn-np:NP76817.RA5DE_20TtxcMzOkUypFgfwEugF0LGZ3iPuHTeCzf49pY130_head
{
this:
np:hasAssertion
dgn-np:NP76817.RA5DE_20TtxcMzOkUypFgfwEugF0LGZ3iPuHTeCzf49pY130_assertion
;
np:hasProvenance
dgn-np:NP76817.RA5DE_20TtxcMzOkUypFgfwEugF0LGZ3iPuHTeCzf49pY130_provenance
;
np:hasPublicationInfo
dgn-np:NP76817.RA5DE_20TtxcMzOkUypFgfwEugF0LGZ3iPuHTeCzf49pY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP76817.RA5DE_20TtxcMzOkUypFgfwEugF0LGZ3iPuHTeCzf49pY130_assertion
a
np:Assertion
.
dgn-np:NP76817.RA5DE_20TtxcMzOkUypFgfwEugF0LGZ3iPuHTeCzf49pY130_provenance
a
np:Provenance
.
dgn-np:NP76817.RA5DE_20TtxcMzOkUypFgfwEugF0LGZ3iPuHTeCzf49pY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP76817.RA5DE_20TtxcMzOkUypFgfwEugF0LGZ3iPuHTeCzf49pY130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGNf49122f61db569cc11bf043a764e08f4
sio:SIO_000628
miriam-gene:1029
,
lld:C0025202
;
a
sio:SIO_001122
.
}
dgn-np:NP76817.RA5DE_20TtxcMzOkUypFgfwEugF0LGZ3iPuHTeCzf49pY130_provenance
{
dgn-np:NP76817.RA5DE_20TtxcMzOkUypFgfwEugF0LGZ3iPuHTeCzf49pY130_assertion
dcterms:description
"[Melanomas were diagnosed only in mutation carriers, and melanoma diagnosis was statistically correlated to the presence of one or more CAN and red hair colour, supporting the possible synergistic effect of a MC1R mutation on increased risk of melanoma in patients with a CDKN2A mutation.]. 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:20526219
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP76817.RA5DE_20TtxcMzOkUypFgfwEugF0LGZ3iPuHTeCzf49pY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:22+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}