@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP648601.RASzkTDedTKWzg7qMJqMK4ZhqTpu_NkQUKFcN2PaeghBg
> .
@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:NP648601.RASzkTDedTKWzg7qMJqMK4ZhqTpu_NkQUKFcN2PaeghBg130_head
{
this:
np:hasAssertion
dgn-np:NP648601.RASzkTDedTKWzg7qMJqMK4ZhqTpu_NkQUKFcN2PaeghBg130_assertion
;
np:hasProvenance
dgn-np:NP648601.RASzkTDedTKWzg7qMJqMK4ZhqTpu_NkQUKFcN2PaeghBg130_provenance
;
np:hasPublicationInfo
dgn-np:NP648601.RASzkTDedTKWzg7qMJqMK4ZhqTpu_NkQUKFcN2PaeghBg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP648601.RASzkTDedTKWzg7qMJqMK4ZhqTpu_NkQUKFcN2PaeghBg130_assertion
a
np:Assertion
.
dgn-np:NP648601.RASzkTDedTKWzg7qMJqMK4ZhqTpu_NkQUKFcN2PaeghBg130_provenance
a
np:Provenance
.
dgn-np:NP648601.RASzkTDedTKWzg7qMJqMK4ZhqTpu_NkQUKFcN2PaeghBg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP648601.RASzkTDedTKWzg7qMJqMK4ZhqTpu_NkQUKFcN2PaeghBg130_assertion
{
miriam-gene:4948
a
ncit:C16612
.
lld:C0001916
a
ncit:C7057
.
dgn-gda:DGNccdf52d8b56524dd2e2bc937a0ff8140
sio:SIO_000628
miriam-gene:4948
,
lld:C0001916
;
a
sio:SIO_001121
.
}
dgn-np:NP648601.RASzkTDedTKWzg7qMJqMK4ZhqTpu_NkQUKFcN2PaeghBg130_provenance
{
dgn-np:NP648601.RASzkTDedTKWzg7qMJqMK4ZhqTpu_NkQUKFcN2PaeghBg130_assertion
dcterms:description
"[The present objectives are to review the literature on albinism (OCA2) in Amerindians, and propose hypotheses for the variable frequencies of the OCA2 gene in Amerindian populations, which include chance processes (founder effect, bottleneck effect, and genetic drift) in small populations, natural selection, cultural selection, and the interaction of situations that led to the increase of the frequency of the albino gene in some generations.]. 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:16369963
;
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:NP648601.RASzkTDedTKWzg7qMJqMK4ZhqTpu_NkQUKFcN2PaeghBg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:30+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" .
}