@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP411971.RAoFJkBitf2bGVdVpc-5ske5jjgapJSHxhKcEX15xf6BE
> .
@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:NP411971.RAoFJkBitf2bGVdVpc-5ske5jjgapJSHxhKcEX15xf6BE130_head
{
this:
np:hasAssertion
dgn-np:NP411971.RAoFJkBitf2bGVdVpc-5ske5jjgapJSHxhKcEX15xf6BE130_assertion
;
np:hasProvenance
dgn-np:NP411971.RAoFJkBitf2bGVdVpc-5ske5jjgapJSHxhKcEX15xf6BE130_provenance
;
np:hasPublicationInfo
dgn-np:NP411971.RAoFJkBitf2bGVdVpc-5ske5jjgapJSHxhKcEX15xf6BE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP411971.RAoFJkBitf2bGVdVpc-5ske5jjgapJSHxhKcEX15xf6BE130_assertion
a
np:Assertion
.
dgn-np:NP411971.RAoFJkBitf2bGVdVpc-5ske5jjgapJSHxhKcEX15xf6BE130_provenance
a
np:Provenance
.
dgn-np:NP411971.RAoFJkBitf2bGVdVpc-5ske5jjgapJSHxhKcEX15xf6BE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP411971.RAoFJkBitf2bGVdVpc-5ske5jjgapJSHxhKcEX15xf6BE130_assertion
{
miriam-gene:4157
a
ncit:C16612
.
lld:C0037284
a
ncit:C7057
.
dgn-gda:DGNa316dc2e32e0e8d758af4f414001fc27
sio:SIO_000628
miriam-gene:4157
,
lld:C0037284
;
a
sio:SIO_001121
.
}
dgn-np:NP411971.RAoFJkBitf2bGVdVpc-5ske5jjgapJSHxhKcEX15xf6BE130_provenance
{
dgn-np:NP411971.RAoFJkBitf2bGVdVpc-5ske5jjgapJSHxhKcEX15xf6BE130_assertion
dcterms:description
"[After adjusting for the effects of pigmentation on the association between MC1R variant alleles and basal cell carcinoma and squamous cell carcinoma risk, the association persisted, confirming that presence of at least one variant allele remains informative in terms of predicting risk for developing a solar-induced skin lesion beyond that information wained through observation of pigmentation phenotype.]. 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:11179997
;
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:NP411971.RAoFJkBitf2bGVdVpc-5ske5jjgapJSHxhKcEX15xf6BE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}