@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg
> .
@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:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_head
{
this:
np:hasAssertion
dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_assertion
;
np:hasProvenance
dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_provenance
;
np:hasPublicationInfo
dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_assertion
a
np:Assertion
.
dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_provenance
a
np:Provenance
.
dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_assertion
{
miriam-gene:1415
a
ncit:C16612
.
lld:C0086543
a
ncit:C7057
.
dgn-gda:DGNdfe26fa2a5c7430d55c0cdf0f8191d8a
sio:SIO_000628
miriam-gene:1415
,
lld:C0086543
;
a
sio:SIO_001121
.
}
dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_provenance
{
dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_assertion
dcterms:description
"[Blood was taken from the proband and his parents, genomic DNA was isolated and some candidate genes for cataract (CRYAA, CRYBB2, GJA8) or macular hypoplasia (OA1, P) or both (PAX6) were analyzed.]. 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:16453125
;
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:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}