@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA
> .
@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:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_head
{
this:
np:hasAssertion
dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_assertion
;
np:hasProvenance
dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_provenance
;
np:hasPublicationInfo
dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_assertion
a
np:Assertion
.
dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_provenance
a
np:Provenance
.
dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_assertion
{
miriam-gene:4157
a
ncit:C16612
.
lld:C0041834
a
ncit:C7057
.
dgn-gda:DGN776b38c1dfad57028039fd3c4aa8e19d
sio:SIO_000628
miriam-gene:4157
,
lld:C0041834
;
a
sio:SIO_001121
.
}
dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_provenance
{
dgn-np:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_assertion
dcterms:description
"[Persons carrying MC1R homozygote variant alleles at R151C, R160W, D294H and D84E were more likely to have fair skin, red hair and to spend less time outdoors than those who did not.]. 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:20129839
;
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:NP653317.RAeyaHP2hX8zf-aFbYritaesDGNO1ym9VnOrMi5L3lHuA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:33+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" .
}