@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP797067.RAo6ivjhxrTXmVTRI2kjO23JQW5PaTDnY2jpaU6rG9jzE
> .
@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:NP797067.RAo6ivjhxrTXmVTRI2kjO23JQW5PaTDnY2jpaU6rG9jzE130_head
{
this:
np:hasAssertion
dgn-np:NP797067.RAo6ivjhxrTXmVTRI2kjO23JQW5PaTDnY2jpaU6rG9jzE130_assertion
;
np:hasProvenance
dgn-np:NP797067.RAo6ivjhxrTXmVTRI2kjO23JQW5PaTDnY2jpaU6rG9jzE130_provenance
;
np:hasPublicationInfo
dgn-np:NP797067.RAo6ivjhxrTXmVTRI2kjO23JQW5PaTDnY2jpaU6rG9jzE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP797067.RAo6ivjhxrTXmVTRI2kjO23JQW5PaTDnY2jpaU6rG9jzE130_assertion
a
np:Assertion
.
dgn-np:NP797067.RAo6ivjhxrTXmVTRI2kjO23JQW5PaTDnY2jpaU6rG9jzE130_provenance
a
np:Provenance
.
dgn-np:NP797067.RAo6ivjhxrTXmVTRI2kjO23JQW5PaTDnY2jpaU6rG9jzE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP797067.RAo6ivjhxrTXmVTRI2kjO23JQW5PaTDnY2jpaU6rG9jzE130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0036421
a
ncit:C7057
.
dgn-gda:DGN23f2f972afa5e8dd06891c2fc88a8b09
sio:SIO_000628
miriam-gene:2944
,
lld:C0036421
;
a
sio:SIO_001121
.
}
dgn-np:NP797067.RAo6ivjhxrTXmVTRI2kjO23JQW5PaTDnY2jpaU6rG9jzE130_provenance
{
dgn-np:NP797067.RAo6ivjhxrTXmVTRI2kjO23JQW5PaTDnY2jpaU6rG9jzE130_assertion
dcterms:description
"[The data show that while M1 and T1 null genotypes were not significantly increased in SSc compared to ethnically matched controls, their frequencies (especially T1 nulls) were significantly higher among SSc patients with hypertension and pulmonary involvement.]. 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:11477481
;
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:NP797067.RAo6ivjhxrTXmVTRI2kjO23JQW5PaTDnY2jpaU6rG9jzE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:09+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" .
}