@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_head
{
this:
np:hasAssertion
dgn-np:NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_assertion
;
np:hasProvenance
dgn-np:NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_provenance
;
np:hasPublicationInfo
dgn-np:NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_assertion
a
np:Assertion
.
dgn-np:NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_provenance
a
np:Provenance
.
dgn-np:NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_assertion
{
miriam-gene:1285
a
ncit:C16612
.
lld:C0403440
a
ncit:C7057
.
dgn-gda:DGN4a88055ef27c2d1d1f31db29dac652f6
sio:SIO_000628
miriam-gene:1285
,
lld:C0403440
;
a
sio:SIO_001121
.
}
dgn-np:NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_provenance
{
dgn-np:NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_assertion
dcterms:description
"[Thirteen unrelated children with TBMN and five individuals with autosomal recessive Alport syndrome were examined for mutations in the 52 exons of COL4A3 and the 47 coding exons of COL4A4 using single-stranded conformation polymorphism (SSCP) analysis.]. 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:17216251
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:44+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}