@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP533901.RAr0f8sXJQTxXjRV5eHKn4H2BG8nQu_w96fK5RI4pa23E
> .
@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:NP533901.RAr0f8sXJQTxXjRV5eHKn4H2BG8nQu_w96fK5RI4pa23E130_head
{
this:
np:hasAssertion
dgn-np:NP533901.RAr0f8sXJQTxXjRV5eHKn4H2BG8nQu_w96fK5RI4pa23E130_assertion
;
np:hasProvenance
dgn-np:NP533901.RAr0f8sXJQTxXjRV5eHKn4H2BG8nQu_w96fK5RI4pa23E130_provenance
;
np:hasPublicationInfo
dgn-np:NP533901.RAr0f8sXJQTxXjRV5eHKn4H2BG8nQu_w96fK5RI4pa23E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP533901.RAr0f8sXJQTxXjRV5eHKn4H2BG8nQu_w96fK5RI4pa23E130_assertion
a
np:Assertion
.
dgn-np:NP533901.RAr0f8sXJQTxXjRV5eHKn4H2BG8nQu_w96fK5RI4pa23E130_provenance
a
np:Provenance
.
dgn-np:NP533901.RAr0f8sXJQTxXjRV5eHKn4H2BG8nQu_w96fK5RI4pa23E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP533901.RAr0f8sXJQTxXjRV5eHKn4H2BG8nQu_w96fK5RI4pa23E130_assertion
{
miriam-gene:4868
a
ncit:C16612
.
lld:C0027726
a
ncit:C7057
.
dgn-gda:DGN3d84752754dc88fafaf01488abca035e
sio:SIO_000628
miriam-gene:4868
,
lld:C0027726
;
a
sio:SIO_001121
.
}
dgn-np:NP533901.RAr0f8sXJQTxXjRV5eHKn4H2BG8nQu_w96fK5RI4pa23E130_provenance
{
dgn-np:NP533901.RAr0f8sXJQTxXjRV5eHKn4H2BG8nQu_w96fK5RI4pa23E130_assertion
dcterms:description
"[Because of its prognostic relevance, we advocate molecular genetic testing of LAMB2 in any case of prenatally detected nephrotic syndrome with negative results of NPHS1 mutational screening, especially in the presence of the typical sonomorphologic findings of the kidneys and the development of oligohydramnios.]. 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:16450351
;
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:NP533901.RAr0f8sXJQTxXjRV5eHKn4H2BG8nQu_w96fK5RI4pa23E130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:46+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" .
}