@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP74460.RAU91_W8_njimpC9tMFhyjCzyDbqdisz6ffqWBR6npCvY
> .
@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:NP74460.RAU91_W8_njimpC9tMFhyjCzyDbqdisz6ffqWBR6npCvY130_head
{
this:
np:hasAssertion
dgn-np:NP74460.RAU91_W8_njimpC9tMFhyjCzyDbqdisz6ffqWBR6npCvY130_assertion
;
np:hasProvenance
dgn-np:NP74460.RAU91_W8_njimpC9tMFhyjCzyDbqdisz6ffqWBR6npCvY130_provenance
;
np:hasPublicationInfo
dgn-np:NP74460.RAU91_W8_njimpC9tMFhyjCzyDbqdisz6ffqWBR6npCvY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP74460.RAU91_W8_njimpC9tMFhyjCzyDbqdisz6ffqWBR6npCvY130_assertion
a
np:Assertion
.
dgn-np:NP74460.RAU91_W8_njimpC9tMFhyjCzyDbqdisz6ffqWBR6npCvY130_provenance
a
np:Provenance
.
dgn-np:NP74460.RAU91_W8_njimpC9tMFhyjCzyDbqdisz6ffqWBR6npCvY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP74460.RAU91_W8_njimpC9tMFhyjCzyDbqdisz6ffqWBR6npCvY130_assertion
{
miriam-gene:2703
a
ncit:C16612
.
lld:C0086543
a
ncit:C7057
.
dgn-gda:DGNd87c7a333364122712ef02bf518e6293
sio:SIO_000628
miriam-gene:2703
,
lld:C0086543
;
a
sio:SIO_001122
.
}
dgn-np:NP74460.RAU91_W8_njimpC9tMFhyjCzyDbqdisz6ffqWBR6npCvY130_provenance
{
dgn-np:NP74460.RAU91_W8_njimpC9tMFhyjCzyDbqdisz6ffqWBR6npCvY130_assertion
dcterms:description
"[Mutation screening was performed in the cataract candidate genes coding for crystallins and connexin 50 by sequencing of polymerase chain reaction (PCR) products amplified from blood leukocyte DNA samples of eight family members.]. 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:18334966
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP74460.RAU91_W8_njimpC9tMFhyjCzyDbqdisz6ffqWBR6npCvY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:36+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" .
}