@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP728851.RAgegwlPPlOaPGNMsBVchLxUBv8N3gmb8IHpqFz_zAhUY
> .
@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:NP728851.RAgegwlPPlOaPGNMsBVchLxUBv8N3gmb8IHpqFz_zAhUY130_head
{
this:
np:hasAssertion
dgn-np:NP728851.RAgegwlPPlOaPGNMsBVchLxUBv8N3gmb8IHpqFz_zAhUY130_assertion
;
np:hasProvenance
dgn-np:NP728851.RAgegwlPPlOaPGNMsBVchLxUBv8N3gmb8IHpqFz_zAhUY130_provenance
;
np:hasPublicationInfo
dgn-np:NP728851.RAgegwlPPlOaPGNMsBVchLxUBv8N3gmb8IHpqFz_zAhUY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP728851.RAgegwlPPlOaPGNMsBVchLxUBv8N3gmb8IHpqFz_zAhUY130_assertion
a
np:Assertion
.
dgn-np:NP728851.RAgegwlPPlOaPGNMsBVchLxUBv8N3gmb8IHpqFz_zAhUY130_provenance
a
np:Provenance
.
dgn-np:NP728851.RAgegwlPPlOaPGNMsBVchLxUBv8N3gmb8IHpqFz_zAhUY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP728851.RAgegwlPPlOaPGNMsBVchLxUBv8N3gmb8IHpqFz_zAhUY130_assertion
{
miriam-gene:161742
a
ncit:C16612
.
lld:C0027831
a
ncit:C7057
.
dgn-gda:DGNa32f4950e378fcb8dde75e5f7d600516
sio:SIO_000628
miriam-gene:161742
,
lld:C0027831
;
a
sio:SIO_001121
.
}
dgn-np:NP728851.RAgegwlPPlOaPGNMsBVchLxUBv8N3gmb8IHpqFz_zAhUY130_provenance
{
dgn-np:NP728851.RAgegwlPPlOaPGNMsBVchLxUBv8N3gmb8IHpqFz_zAhUY130_assertion
dcterms:description
"[Patients fulfilling the National Institutes of Health (NIH) diagnostic criteria for NF1 were enrolled at the University of Utah NF Clinic, and SPRED1 mutation analysis was performed to identify the frequency of Legius syndrome within an NF1 clinic population.]. 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:20179001
;
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:NP728851.RAgegwlPPlOaPGNMsBVchLxUBv8N3gmb8IHpqFz_zAhUY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:22+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" .
}