@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP869200.RARTk7h46EuvMoKh7jjJXwQ1BNxRnBZzW2HclQvqnbzeY
> .
@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:NP869200.RARTk7h46EuvMoKh7jjJXwQ1BNxRnBZzW2HclQvqnbzeY130_head
{
this:
np:hasAssertion
dgn-np:NP869200.RARTk7h46EuvMoKh7jjJXwQ1BNxRnBZzW2HclQvqnbzeY130_assertion
;
np:hasProvenance
dgn-np:NP869200.RARTk7h46EuvMoKh7jjJXwQ1BNxRnBZzW2HclQvqnbzeY130_provenance
;
np:hasPublicationInfo
dgn-np:NP869200.RARTk7h46EuvMoKh7jjJXwQ1BNxRnBZzW2HclQvqnbzeY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP869200.RARTk7h46EuvMoKh7jjJXwQ1BNxRnBZzW2HclQvqnbzeY130_assertion
a
np:Assertion
.
dgn-np:NP869200.RARTk7h46EuvMoKh7jjJXwQ1BNxRnBZzW2HclQvqnbzeY130_provenance
a
np:Provenance
.
dgn-np:NP869200.RARTk7h46EuvMoKh7jjJXwQ1BNxRnBZzW2HclQvqnbzeY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP869200.RARTk7h46EuvMoKh7jjJXwQ1BNxRnBZzW2HclQvqnbzeY130_assertion
{
miriam-gene:10161
a
ncit:C16612
.
lld:C0020678
a
ncit:C7057
.
dgn-gda:DGNbbbf204c8f8563787c70c9933b9e9a6a
sio:SIO_000628
miriam-gene:10161
,
lld:C0020678
;
a
sio:SIO_001121
.
}
dgn-np:NP869200.RARTk7h46EuvMoKh7jjJXwQ1BNxRnBZzW2HclQvqnbzeY130_provenance
{
dgn-np:NP869200.RARTk7h46EuvMoKh7jjJXwQ1BNxRnBZzW2HclQvqnbzeY130_assertion
dcterms:description
"[Our findings show that mutations in P2RY5 display variable expressivity, underlying both hypotrichosis and woolly hair, and underscore the essential role of P2RY5 in the tissue integrity and maintenance of the hair follicle.]. 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:18692127
;
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:NP869200.RARTk7h46EuvMoKh7jjJXwQ1BNxRnBZzW2HclQvqnbzeY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:51+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" .
}