@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP875424.RA3JYI-WbvyqdynAvKjYBbK_3IHM1ai4IDTs2wWNXI0IE
> .
@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:NP875424.RA3JYI-WbvyqdynAvKjYBbK_3IHM1ai4IDTs2wWNXI0IE130_head
{
this:
np:hasAssertion
dgn-np:NP875424.RA3JYI-WbvyqdynAvKjYBbK_3IHM1ai4IDTs2wWNXI0IE130_assertion
;
np:hasProvenance
dgn-np:NP875424.RA3JYI-WbvyqdynAvKjYBbK_3IHM1ai4IDTs2wWNXI0IE130_provenance
;
np:hasPublicationInfo
dgn-np:NP875424.RA3JYI-WbvyqdynAvKjYBbK_3IHM1ai4IDTs2wWNXI0IE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP875424.RA3JYI-WbvyqdynAvKjYBbK_3IHM1ai4IDTs2wWNXI0IE130_assertion
a
np:Assertion
.
dgn-np:NP875424.RA3JYI-WbvyqdynAvKjYBbK_3IHM1ai4IDTs2wWNXI0IE130_provenance
a
np:Provenance
.
dgn-np:NP875424.RA3JYI-WbvyqdynAvKjYBbK_3IHM1ai4IDTs2wWNXI0IE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP875424.RA3JYI-WbvyqdynAvKjYBbK_3IHM1ai4IDTs2wWNXI0IE130_assertion
{
miriam-gene:100128922
a
ncit:C16612
.
lld:C0009691
a
ncit:C7057
.
dgn-gda:DGN7c76c2bb144585f1807b4d3a2cfa04fb
sio:SIO_000628
miriam-gene:100128922
,
lld:C0009691
;
a
sio:SIO_001121
.
}
dgn-np:NP875424.RA3JYI-WbvyqdynAvKjYBbK_3IHM1ai4IDTs2wWNXI0IE130_provenance
{
dgn-np:NP875424.RA3JYI-WbvyqdynAvKjYBbK_3IHM1ai4IDTs2wWNXI0IE130_assertion
dcterms:description
"[In the last decade or so, increasing evidences suggest that the mutations of two connexin genes, GJA3 and GJA8, are directly linked to human congenital cataracts in North and Central America, Europe and Asia.]. 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:21091421
;
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:NP875424.RA3JYI-WbvyqdynAvKjYBbK_3IHM1ai4IDTs2wWNXI0IE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:55+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" .
}