@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP722442.RAUov_4P2uvjyKmm76OtTaDf6UmYQBJnWm8OyadZN7EKA
> .
@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:NP722442.RAUov_4P2uvjyKmm76OtTaDf6UmYQBJnWm8OyadZN7EKA130_head
{
this:
np:hasAssertion
dgn-np:NP722442.RAUov_4P2uvjyKmm76OtTaDf6UmYQBJnWm8OyadZN7EKA130_assertion
;
np:hasProvenance
dgn-np:NP722442.RAUov_4P2uvjyKmm76OtTaDf6UmYQBJnWm8OyadZN7EKA130_provenance
;
np:hasPublicationInfo
dgn-np:NP722442.RAUov_4P2uvjyKmm76OtTaDf6UmYQBJnWm8OyadZN7EKA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP722442.RAUov_4P2uvjyKmm76OtTaDf6UmYQBJnWm8OyadZN7EKA130_assertion
a
np:Assertion
.
dgn-np:NP722442.RAUov_4P2uvjyKmm76OtTaDf6UmYQBJnWm8OyadZN7EKA130_provenance
a
np:Provenance
.
dgn-np:NP722442.RAUov_4P2uvjyKmm76OtTaDf6UmYQBJnWm8OyadZN7EKA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP722442.RAUov_4P2uvjyKmm76OtTaDf6UmYQBJnWm8OyadZN7EKA130_assertion
{
miriam-gene:7299
a
ncit:C16612
.
lld:C0032897
a
ncit:C7057
.
dgn-gda:DGNdf051ded8ec35e2eed53fcf94286a964
sio:SIO_000628
miriam-gene:7299
,
lld:C0032897
;
a
sio:SIO_001121
.
}
dgn-np:NP722442.RAUov_4P2uvjyKmm76OtTaDf6UmYQBJnWm8OyadZN7EKA130_provenance
{
dgn-np:NP722442.RAUov_4P2uvjyKmm76OtTaDf6UmYQBJnWm8OyadZN7EKA130_assertion
dcterms:description
"[Hypopigmentation characterized by light skin, reduced retinal pigment, low hairbulb tyrosinase activity, and incomplete melanization of melanosomes is part of the phenotype of AS, and is similar to that found in PWS.]. 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:8494033
;
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:NP722442.RAUov_4P2uvjyKmm76OtTaDf6UmYQBJnWm8OyadZN7EKA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:18+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" .
}