@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP77319.RAL0a8U9KIm285oBZb7vvRfkHcNcb-q6O50OO3NHQwRFA
> .
@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:NP77319.RAL0a8U9KIm285oBZb7vvRfkHcNcb-q6O50OO3NHQwRFA130_head
{
this:
np:hasAssertion
dgn-np:NP77319.RAL0a8U9KIm285oBZb7vvRfkHcNcb-q6O50OO3NHQwRFA130_assertion
;
np:hasProvenance
dgn-np:NP77319.RAL0a8U9KIm285oBZb7vvRfkHcNcb-q6O50OO3NHQwRFA130_provenance
;
np:hasPublicationInfo
dgn-np:NP77319.RAL0a8U9KIm285oBZb7vvRfkHcNcb-q6O50OO3NHQwRFA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP77319.RAL0a8U9KIm285oBZb7vvRfkHcNcb-q6O50OO3NHQwRFA130_assertion
a
np:Assertion
.
dgn-np:NP77319.RAL0a8U9KIm285oBZb7vvRfkHcNcb-q6O50OO3NHQwRFA130_provenance
a
np:Provenance
.
dgn-np:NP77319.RAL0a8U9KIm285oBZb7vvRfkHcNcb-q6O50OO3NHQwRFA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP77319.RAL0a8U9KIm285oBZb7vvRfkHcNcb-q6O50OO3NHQwRFA130_assertion
{
miriam-gene:1286
a
ncit:C16612
.
lld:C0022578
a
ncit:C7057
.
dgn-gda:DGN8c62f1d2cbab8a31581cf4f4bacc2e57
sio:SIO_000628
miriam-gene:1286
,
lld:C0022578
;
a
sio:SIO_001122
.
}
dgn-np:NP77319.RAL0a8U9KIm285oBZb7vvRfkHcNcb-q6O50OO3NHQwRFA130_provenance
{
dgn-np:NP77319.RAL0a8U9KIm285oBZb7vvRfkHcNcb-q6O50OO3NHQwRFA130_assertion
dcterms:description
"[Analysis of COL4A3 and COL4A4 revealed no mutations related to KC patients, but specific genotypes of seven previously described polymorphisms are significantly associated with KC under dominant, recessive, or additive models.]. 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:20029656
;
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:NP77319.RAL0a8U9KIm285oBZb7vvRfkHcNcb-q6O50OO3NHQwRFA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:37+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" .
}