@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP430604.RAkUWWxRuAHNaKOJrrLH4J7OGhDYPmHVVCZRHzIf-BdQE
> .
@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:NP430604.RAkUWWxRuAHNaKOJrrLH4J7OGhDYPmHVVCZRHzIf-BdQE130_head
{
this:
np:hasAssertion
dgn-np:NP430604.RAkUWWxRuAHNaKOJrrLH4J7OGhDYPmHVVCZRHzIf-BdQE130_assertion
;
np:hasProvenance
dgn-np:NP430604.RAkUWWxRuAHNaKOJrrLH4J7OGhDYPmHVVCZRHzIf-BdQE130_provenance
;
np:hasPublicationInfo
dgn-np:NP430604.RAkUWWxRuAHNaKOJrrLH4J7OGhDYPmHVVCZRHzIf-BdQE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP430604.RAkUWWxRuAHNaKOJrrLH4J7OGhDYPmHVVCZRHzIf-BdQE130_assertion
a
np:Assertion
.
dgn-np:NP430604.RAkUWWxRuAHNaKOJrrLH4J7OGhDYPmHVVCZRHzIf-BdQE130_provenance
a
np:Provenance
.
dgn-np:NP430604.RAkUWWxRuAHNaKOJrrLH4J7OGhDYPmHVVCZRHzIf-BdQE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP430604.RAkUWWxRuAHNaKOJrrLH4J7OGhDYPmHVVCZRHzIf-BdQE130_assertion
{
miriam-gene:1285
a
ncit:C16612
.
lld:C1563715
a
ncit:C7057
.
dgn-gda:DGN9972170f6d446af05c452a7da5905640
sio:SIO_000628
miriam-gene:1285
,
lld:C1563715
;
a
sio:SIO_001121
.
}
dgn-np:NP430604.RAkUWWxRuAHNaKOJrrLH4J7OGhDYPmHVVCZRHzIf-BdQE130_provenance
{
dgn-np:NP430604.RAkUWWxRuAHNaKOJrrLH4J7OGhDYPmHVVCZRHzIf-BdQE130_assertion
dcterms:description
"[A clinical evaluation of probands and their relatives of the five families carrying mutations in either the COL4A3 or the COL4A4 gene was carried out to underline the natural history of the autosomal recessive ATS.]. 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:16338941
;
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:NP430604.RAkUWWxRuAHNaKOJrrLH4J7OGhDYPmHVVCZRHzIf-BdQE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+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" .
}