@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP637179.RA_6f4fnxAbHdsT26BWq9snYdlwGVDBesyNmApU_OvB30
> .
@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:NP637179.RA_6f4fnxAbHdsT26BWq9snYdlwGVDBesyNmApU_OvB30130_head
{
this:
np:hasAssertion
dgn-np:NP637179.RA_6f4fnxAbHdsT26BWq9snYdlwGVDBesyNmApU_OvB30130_assertion
;
np:hasProvenance
dgn-np:NP637179.RA_6f4fnxAbHdsT26BWq9snYdlwGVDBesyNmApU_OvB30130_provenance
;
np:hasPublicationInfo
dgn-np:NP637179.RA_6f4fnxAbHdsT26BWq9snYdlwGVDBesyNmApU_OvB30130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP637179.RA_6f4fnxAbHdsT26BWq9snYdlwGVDBesyNmApU_OvB30130_assertion
a
np:Assertion
.
dgn-np:NP637179.RA_6f4fnxAbHdsT26BWq9snYdlwGVDBesyNmApU_OvB30130_provenance
a
np:Provenance
.
dgn-np:NP637179.RA_6f4fnxAbHdsT26BWq9snYdlwGVDBesyNmApU_OvB30130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP637179.RA_6f4fnxAbHdsT26BWq9snYdlwGVDBesyNmApU_OvB30130_assertion
{
miriam-gene:57216
a
ncit:C16612
.
lld:C0028738
a
ncit:C7057
.
dgn-gda:DGN839bc12626f026cfe87feb1c97b73b3e
sio:SIO_000628
miriam-gene:57216
,
lld:C0028738
;
a
sio:SIO_001121
.
}
dgn-np:NP637179.RA_6f4fnxAbHdsT26BWq9snYdlwGVDBesyNmApU_OvB30130_provenance
{
dgn-np:NP637179.RA_6f4fnxAbHdsT26BWq9snYdlwGVDBesyNmApU_OvB30130_assertion
dcterms:description
"[The phenotype for different types of albinism varies according to the amount of pigment in the hale, skin and iris, the reduction in visual acuity and the degree of nystagmus and strabismus.]. 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:8719278
;
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:NP637179.RA_6f4fnxAbHdsT26BWq9snYdlwGVDBesyNmApU_OvB30130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:24+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" .
}