@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1106670.RAR5L17IbV0YCzeN8A8UZZ0N8yaMIAzAYIv-by_s-c5jk
> .
@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/v4.0.0/void/
> .
dgn-np:NP1106670.RAR5L17IbV0YCzeN8A8UZZ0N8yaMIAzAYIv-by_s-c5jk130_head
{
this:
np:hasAssertion
dgn-np:NP1106670.RAR5L17IbV0YCzeN8A8UZZ0N8yaMIAzAYIv-by_s-c5jk130_assertion
;
np:hasProvenance
dgn-np:NP1106670.RAR5L17IbV0YCzeN8A8UZZ0N8yaMIAzAYIv-by_s-c5jk130_provenance
;
np:hasPublicationInfo
dgn-np:NP1106670.RAR5L17IbV0YCzeN8A8UZZ0N8yaMIAzAYIv-by_s-c5jk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1106670.RAR5L17IbV0YCzeN8A8UZZ0N8yaMIAzAYIv-by_s-c5jk130_assertion
a
np:Assertion
.
dgn-np:NP1106670.RAR5L17IbV0YCzeN8A8UZZ0N8yaMIAzAYIv-by_s-c5jk130_provenance
a
np:Provenance
.
dgn-np:NP1106670.RAR5L17IbV0YCzeN8A8UZZ0N8yaMIAzAYIv-by_s-c5jk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1106670.RAR5L17IbV0YCzeN8A8UZZ0N8yaMIAzAYIv-by_s-c5jk130_assertion
{
miriam-gene:4036
a
ncit:C16612
.
lld:C0175754
a
ncit:C7057
.
dgn-gda:DGNe8669219cf202dd056e9f3f89b5d40a9
sio:SIO_000628
miriam-gene:4036
,
lld:C0175754
;
a
sio:SIO_001121
.
}
dgn-np:NP1106670.RAR5L17IbV0YCzeN8A8UZZ0N8yaMIAzAYIv-by_s-c5jk130_provenance
{
dgn-np:NP1106670.RAR5L17IbV0YCzeN8A8UZZ0N8yaMIAzAYIv-by_s-c5jk130_assertion
dcterms:description
"[Mutations in LRP2 have been shown to cause the Donnai-Barrow syndrome (DBS) or facio-oculo-acoustico-renal (FOAR) syndrome, a syndrome associated with facial dysmorphism, ocular anomalies, sensorineural hearing loss, low molecular weight proteinuria, and diaphragmatic hernia and absent corpus callosum, although there is variability in the expression of some features.]. 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:23992033
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1106670.RAR5L17IbV0YCzeN8A8UZZ0N8yaMIAzAYIv-by_s-c5jk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:07+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}