@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP568777.RAjAvUivq4tHvyBjh3tzRSw1KUeufOgZsMAlm859o6fws
> .
@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:NP568777.RAjAvUivq4tHvyBjh3tzRSw1KUeufOgZsMAlm859o6fws130_head
{
this:
np:hasAssertion
dgn-np:NP568777.RAjAvUivq4tHvyBjh3tzRSw1KUeufOgZsMAlm859o6fws130_assertion
;
np:hasProvenance
dgn-np:NP568777.RAjAvUivq4tHvyBjh3tzRSw1KUeufOgZsMAlm859o6fws130_provenance
;
np:hasPublicationInfo
dgn-np:NP568777.RAjAvUivq4tHvyBjh3tzRSw1KUeufOgZsMAlm859o6fws130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP568777.RAjAvUivq4tHvyBjh3tzRSw1KUeufOgZsMAlm859o6fws130_assertion
a
np:Assertion
.
dgn-np:NP568777.RAjAvUivq4tHvyBjh3tzRSw1KUeufOgZsMAlm859o6fws130_provenance
a
np:Provenance
.
dgn-np:NP568777.RAjAvUivq4tHvyBjh3tzRSw1KUeufOgZsMAlm859o6fws130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP568777.RAjAvUivq4tHvyBjh3tzRSw1KUeufOgZsMAlm859o6fws130_assertion
{
miriam-gene:5894
a
ncit:C16612
.
lld:C0175704
a
ncit:C7057
.
dgn-gda:DGN02f9a13fa17b35c93790f0b0c250f676
sio:SIO_000628
miriam-gene:5894
,
lld:C0175704
;
a
sio:SIO_001121
.
}
dgn-np:NP568777.RAjAvUivq4tHvyBjh3tzRSw1KUeufOgZsMAlm859o6fws130_provenance
{
dgn-np:NP568777.RAjAvUivq4tHvyBjh3tzRSw1KUeufOgZsMAlm859o6fws130_assertion
dcterms:description
"[The aim of the study was to assess various aspects of visual and visuoperceptual function in patients with Noonan syndrome (NS) or LEOPARD syndrome (LS) with mutations affecting the PTPN11, SOS1 and RAF1 genes.]. 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:19568997
;
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:NP568777.RAjAvUivq4tHvyBjh3tzRSw1KUeufOgZsMAlm859o6fws130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:43+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" .
}