@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP716718.RAAm_C3Vi6SQsUykj-G4-uR0mx2Or3C89id71kUyNwFDQ
> .
@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:NP716718.RAAm_C3Vi6SQsUykj-G4-uR0mx2Or3C89id71kUyNwFDQ130_head
{
this:
np:hasAssertion
dgn-np:NP716718.RAAm_C3Vi6SQsUykj-G4-uR0mx2Or3C89id71kUyNwFDQ130_assertion
;
np:hasProvenance
dgn-np:NP716718.RAAm_C3Vi6SQsUykj-G4-uR0mx2Or3C89id71kUyNwFDQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP716718.RAAm_C3Vi6SQsUykj-G4-uR0mx2Or3C89id71kUyNwFDQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP716718.RAAm_C3Vi6SQsUykj-G4-uR0mx2Or3C89id71kUyNwFDQ130_assertion
a
np:Assertion
.
dgn-np:NP716718.RAAm_C3Vi6SQsUykj-G4-uR0mx2Or3C89id71kUyNwFDQ130_provenance
a
np:Provenance
.
dgn-np:NP716718.RAAm_C3Vi6SQsUykj-G4-uR0mx2Or3C89id71kUyNwFDQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP716718.RAAm_C3Vi6SQsUykj-G4-uR0mx2Or3C89id71kUyNwFDQ130_assertion
{
miriam-gene:6591
a
ncit:C16612
.
lld:C0080024
a
ncit:C7057
.
dgn-gda:DGNd908b0473a47bbc9e22b01b5d6d28f78
sio:SIO_000628
miriam-gene:6591
,
lld:C0080024
;
a
sio:SIO_001121
.
}
dgn-np:NP716718.RAAm_C3Vi6SQsUykj-G4-uR0mx2Or3C89id71kUyNwFDQ130_provenance
{
dgn-np:NP716718.RAAm_C3Vi6SQsUykj-G4-uR0mx2Or3C89id71kUyNwFDQ130_assertion
dcterms:description
"[To investigate the possibility that some cases of human piebaldism might result from abnormalities of the human SLUG (SNAI2) gene, we carried out Southern blot analysis of the SLUG gene in 17 unrelated patients with piebaldism, who lack apparent KIT mutations.]. 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:12955764
;
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:NP716718.RAAm_C3Vi6SQsUykj-G4-uR0mx2Or3C89id71kUyNwFDQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:15+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" .
}