@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP712956.RAKN8EQQRYObP9PfhnERQGHtm1_ETocAeGVNbYp_alV1w
> .
@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:NP712956.RAKN8EQQRYObP9PfhnERQGHtm1_ETocAeGVNbYp_alV1w130_head
{
this:
np:hasAssertion
dgn-np:NP712956.RAKN8EQQRYObP9PfhnERQGHtm1_ETocAeGVNbYp_alV1w130_assertion
;
np:hasProvenance
dgn-np:NP712956.RAKN8EQQRYObP9PfhnERQGHtm1_ETocAeGVNbYp_alV1w130_provenance
;
np:hasPublicationInfo
dgn-np:NP712956.RAKN8EQQRYObP9PfhnERQGHtm1_ETocAeGVNbYp_alV1w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP712956.RAKN8EQQRYObP9PfhnERQGHtm1_ETocAeGVNbYp_alV1w130_assertion
a
np:Assertion
.
dgn-np:NP712956.RAKN8EQQRYObP9PfhnERQGHtm1_ETocAeGVNbYp_alV1w130_provenance
a
np:Provenance
.
dgn-np:NP712956.RAKN8EQQRYObP9PfhnERQGHtm1_ETocAeGVNbYp_alV1w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP712956.RAKN8EQQRYObP9PfhnERQGHtm1_ETocAeGVNbYp_alV1w130_assertion
{
miriam-gene:10950
a
ncit:C16612
.
lld:C0039446
a
ncit:C7057
.
dgn-gda:DGNd9dfdccf52c96c15d5ab728a5a05379f
sio:SIO_000628
miriam-gene:10950
,
lld:C0039446
;
a
sio:SIO_001121
.
}
dgn-np:NP712956.RAKN8EQQRYObP9PfhnERQGHtm1_ETocAeGVNbYp_alV1w130_provenance
{
dgn-np:NP712956.RAKN8EQQRYObP9PfhnERQGHtm1_ETocAeGVNbYp_alV1w130_assertion
dcterms:description
"[Because the telangiectasia of hereditary hemorrhagic telangiectasia (HHT) and the CREST variant of scleroderma may be indistinguishable, we have tested the sera of eight patients with HHT for the presence of antinuclear (ANA) and anticentromere antibodies (ACA).]. 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:6609175
;
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:NP712956.RAKN8EQQRYObP9PfhnERQGHtm1_ETocAeGVNbYp_alV1w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:13+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" .
}