@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP276582.RAIeX6hR0yj9o0j_olsjHxx2k2ataAMGMsl64DEfv5rsQ
> .
@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:NP276582.RAIeX6hR0yj9o0j_olsjHxx2k2ataAMGMsl64DEfv5rsQ130_head
{
this:
np:hasAssertion
dgn-np:NP276582.RAIeX6hR0yj9o0j_olsjHxx2k2ataAMGMsl64DEfv5rsQ130_assertion
;
np:hasProvenance
dgn-np:NP276582.RAIeX6hR0yj9o0j_olsjHxx2k2ataAMGMsl64DEfv5rsQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP276582.RAIeX6hR0yj9o0j_olsjHxx2k2ataAMGMsl64DEfv5rsQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP276582.RAIeX6hR0yj9o0j_olsjHxx2k2ataAMGMsl64DEfv5rsQ130_assertion
a
np:Assertion
.
dgn-np:NP276582.RAIeX6hR0yj9o0j_olsjHxx2k2ataAMGMsl64DEfv5rsQ130_provenance
a
np:Provenance
.
dgn-np:NP276582.RAIeX6hR0yj9o0j_olsjHxx2k2ataAMGMsl64DEfv5rsQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP276582.RAIeX6hR0yj9o0j_olsjHxx2k2ataAMGMsl64DEfv5rsQ130_assertion
{
miriam-gene:26039
a
ncit:C16612
.
lld:C0006664
a
ncit:C7057
.
dgn-gda:DGN82dbda8dbf1377f3adaa10334a974517
sio:SIO_000628
miriam-gene:26039
,
lld:C0006664
;
a
sio:SIO_001121
.
}
dgn-np:NP276582.RAIeX6hR0yj9o0j_olsjHxx2k2ataAMGMsl64DEfv5rsQ130_provenance
{
dgn-np:NP276582.RAIeX6hR0yj9o0j_olsjHxx2k2ataAMGMsl64DEfv5rsQ130_assertion
dcterms:description
"[Clinical features of the CREST (calcinosis cutis, Raynaud's syndrome, esophageal dysmotility, sclerodactyly, and telangiectasias) syndrome are sometimes exhibited in patients with primary biliary cirrhosis (PBC), but the postulated autoimmune mechanisms behind these conditions are poorly understood.]. 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:10347101
;
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:NP276582.RAIeX6hR0yj9o0j_olsjHxx2k2ataAMGMsl64DEfv5rsQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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" .
}