@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0
> .
@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:NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_head
{
this:
np:hasAssertion
dgn-np:NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_assertion
;
np:hasProvenance
dgn-np:NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_provenance
;
np:hasPublicationInfo
dgn-np:NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_assertion
a
np:Assertion
.
dgn-np:NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_provenance
a
np:Provenance
.
dgn-np:NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_assertion
{
miriam-gene:5167
a
ncit:C16612
.
lld:C0033847
a
ncit:C7057
.
dgn-gda:DGNc7862a7b3d5257c87a7b1107a9be3f2c
sio:SIO_000628
miriam-gene:5167
,
lld:C0033847
;
a
sio:SIO_001121
.
}
dgn-np:NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_provenance
{
dgn-np:NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_assertion
dcterms:description
"[This report emphasizes concurrently that ABCC6 may be a relevant candidate gene in some cases of GACI with no mutations in the ENPP1 gene, and that GACI may be an atypical and severe end of the vascular phenotype spectrum of PXE.]. 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:20034067
;
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:NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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" .
}