@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP68975.RA8qTGGDt-9RZbYQEqDof0pX9ScEI53tkwyG0OtK6cfaM
> .
@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:NP68975.RA8qTGGDt-9RZbYQEqDof0pX9ScEI53tkwyG0OtK6cfaM130_head
{
this:
np:hasAssertion
dgn-np:NP68975.RA8qTGGDt-9RZbYQEqDof0pX9ScEI53tkwyG0OtK6cfaM130_assertion
;
np:hasProvenance
dgn-np:NP68975.RA8qTGGDt-9RZbYQEqDof0pX9ScEI53tkwyG0OtK6cfaM130_provenance
;
np:hasPublicationInfo
dgn-np:NP68975.RA8qTGGDt-9RZbYQEqDof0pX9ScEI53tkwyG0OtK6cfaM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP68975.RA8qTGGDt-9RZbYQEqDof0pX9ScEI53tkwyG0OtK6cfaM130_assertion
a
np:Assertion
.
dgn-np:NP68975.RA8qTGGDt-9RZbYQEqDof0pX9ScEI53tkwyG0OtK6cfaM130_provenance
a
np:Provenance
.
dgn-np:NP68975.RA8qTGGDt-9RZbYQEqDof0pX9ScEI53tkwyG0OtK6cfaM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP68975.RA8qTGGDt-9RZbYQEqDof0pX9ScEI53tkwyG0OtK6cfaM130_assertion
{
miriam-gene:4157
a
ncit:C16612
.
lld:C0016689
a
ncit:C7057
.
dgn-gda:DGN4292c44402c351351901888f5e31f894
sio:SIO_000628
miriam-gene:4157
,
lld:C0016689
;
a
sio:SIO_001122
.
}
dgn-np:NP68975.RA8qTGGDt-9RZbYQEqDof0pX9ScEI53tkwyG0OtK6cfaM130_provenance
{
dgn-np:NP68975.RA8qTGGDt-9RZbYQEqDof0pX9ScEI53tkwyG0OtK6cfaM130_assertion
dcterms:description
"[As nearly all individuals with ephelides were carriers of at least one MC1R gene variant, our data suggest that MC1R gene variants are necessary to develop ephelides. The results of the study also suggest that MC1R gene variants play a role, although less]. 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:11487574
;
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:NP68975.RA8qTGGDt-9RZbYQEqDof0pX9ScEI53tkwyG0OtK6cfaM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:17+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" .
}