@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg
> .
@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:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_head
{
this:
np:hasAssertion
dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_assertion
;
np:hasProvenance
dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_provenance
;
np:hasPublicationInfo
dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_assertion
a
np:Assertion
.
dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_provenance
a
np:Provenance
.
dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_assertion
{
miriam-gene:10161
a
ncit:C16612
.
lld:C0018500
a
ncit:C7057
.
dgn-gda:DGN7841f6418ea22663081f6f851d2cc55b
sio:SIO_000628
miriam-gene:10161
,
lld:C0018500
;
a
sio:SIO_001121
.
}
dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_provenance
{
dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_assertion
dcterms:description
"[Although these findings clearly reveal the involvement of P2RY5 mutations in hereditary hair diseases, the clinical manifestations of P2RY5 mutations have not completely been elucidated because of limited information to date.]. 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:18803659
;
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:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:51+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" .
}