@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c
> .
@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:NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_head
{
this:
np:hasAssertion
dgn-np:NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_assertion
;
np:hasProvenance
dgn-np:NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_provenance
;
np:hasPublicationInfo
dgn-np:NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_assertion
a
np:Assertion
.
dgn-np:NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_provenance
a
np:Provenance
.
dgn-np:NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_assertion
{
miriam-gene:1287
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGN199bdaca88611822213c743f8206fad4
sio:SIO_000628
miriam-gene:1287
,
lld:C0022658
;
a
sio:SIO_001121
.
}
dgn-np:NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_provenance
{
dgn-np:NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_assertion
dcterms:description
"[This mutation, in a non-collagenous interruption associated with severe renal disease, provides evidence for the importance of this structural motif and suggests the range of phenotypes associated with COL4A5 mutations is more diverse than previously realized.]. 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:20881942
;
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:NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:22+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" .
}