@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP826345.RAEAF5SChzgVGmVuw4hEEI_iqb6UEuGzcYKA0iuj7tglc
> .
@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:NP826345.RAEAF5SChzgVGmVuw4hEEI_iqb6UEuGzcYKA0iuj7tglc130_head
{
this:
np:hasAssertion
dgn-np:NP826345.RAEAF5SChzgVGmVuw4hEEI_iqb6UEuGzcYKA0iuj7tglc130_assertion
;
np:hasProvenance
dgn-np:NP826345.RAEAF5SChzgVGmVuw4hEEI_iqb6UEuGzcYKA0iuj7tglc130_provenance
;
np:hasPublicationInfo
dgn-np:NP826345.RAEAF5SChzgVGmVuw4hEEI_iqb6UEuGzcYKA0iuj7tglc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP826345.RAEAF5SChzgVGmVuw4hEEI_iqb6UEuGzcYKA0iuj7tglc130_assertion
a
np:Assertion
.
dgn-np:NP826345.RAEAF5SChzgVGmVuw4hEEI_iqb6UEuGzcYKA0iuj7tglc130_provenance
a
np:Provenance
.
dgn-np:NP826345.RAEAF5SChzgVGmVuw4hEEI_iqb6UEuGzcYKA0iuj7tglc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP826345.RAEAF5SChzgVGmVuw4hEEI_iqb6UEuGzcYKA0iuj7tglc130_assertion
{
miriam-gene:54751
a
ncit:C16612
.
lld:C0848332
a
ncit:C7057
.
dgn-gda:DGNfc10534ce60937e495a9af6a6aa201dc
sio:SIO_000628
miriam-gene:54751
,
lld:C0848332
;
a
sio:SIO_001121
.
}
dgn-np:NP826345.RAEAF5SChzgVGmVuw4hEEI_iqb6UEuGzcYKA0iuj7tglc130_provenance
{
dgn-np:NP826345.RAEAF5SChzgVGmVuw4hEEI_iqb6UEuGzcYKA0iuj7tglc130_assertion
dcterms:description
"[In assessing children of an affected patient, those who have inherited the gene can be distinguished from their normal sibs on the basis of whether or not café au lait (CAL) spots are present by the age of five years.]. 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:2511319
;
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:NP826345.RAEAF5SChzgVGmVuw4hEEI_iqb6UEuGzcYKA0iuj7tglc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:26+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" .
}