@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP308794.RAtpOto63cSTqmx3YNbG9vbtedcSDf0h7i9BLSKj__UbQ
> .
@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:NP308794.RAtpOto63cSTqmx3YNbG9vbtedcSDf0h7i9BLSKj__UbQ130_head
{
this:
np:hasAssertion
dgn-np:NP308794.RAtpOto63cSTqmx3YNbG9vbtedcSDf0h7i9BLSKj__UbQ130_assertion
;
np:hasProvenance
dgn-np:NP308794.RAtpOto63cSTqmx3YNbG9vbtedcSDf0h7i9BLSKj__UbQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP308794.RAtpOto63cSTqmx3YNbG9vbtedcSDf0h7i9BLSKj__UbQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP308794.RAtpOto63cSTqmx3YNbG9vbtedcSDf0h7i9BLSKj__UbQ130_assertion
a
np:Assertion
.
dgn-np:NP308794.RAtpOto63cSTqmx3YNbG9vbtedcSDf0h7i9BLSKj__UbQ130_provenance
a
np:Provenance
.
dgn-np:NP308794.RAtpOto63cSTqmx3YNbG9vbtedcSDf0h7i9BLSKj__UbQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP308794.RAtpOto63cSTqmx3YNbG9vbtedcSDf0h7i9BLSKj__UbQ130_assertion
{
miriam-gene:4157
a
ncit:C16612
.
lld:C0027962
a
ncit:C7057
.
dgn-gda:DGN4edd10426ca1c00b8cf6a17a427056ae
sio:SIO_000628
miriam-gene:4157
,
lld:C0027962
;
a
sio:SIO_001121
.
}
dgn-np:NP308794.RAtpOto63cSTqmx3YNbG9vbtedcSDf0h7i9BLSKj__UbQ130_provenance
{
dgn-np:NP308794.RAtpOto63cSTqmx3YNbG9vbtedcSDf0h7i9BLSKj__UbQ130_assertion
dcterms:description
"[The relationships between MC1R gene variants and red hair, skin reflectance, degree of freckling and nevus count were investigated in 2331 adolescent twins, their sibs and parents in 645 twin families.]. 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:14709592
;
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:NP308794.RAtpOto63cSTqmx3YNbG9vbtedcSDf0h7i9BLSKj__UbQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:57+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" .
}