@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA
> .
@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:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_head
{
this:
np:hasAssertion
dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_assertion
;
np:hasProvenance
dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_provenance
;
np:hasPublicationInfo
dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_assertion
a
np:Assertion
.
dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_provenance
a
np:Provenance
.
dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_assertion
{
miriam-gene:2335
a
ncit:C16612
.
lld:C0410179
a
ncit:C7057
.
dgn-gda:DGN74cfbf6314176040d095e8bf672bbf26
sio:SIO_000628
miriam-gene:2335
,
lld:C0410179
;
a
sio:SIO_001121
.
}
dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_provenance
{
dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_assertion
dcterms:description
"[Recently we found a marked reduction of fibronectin receptors in the skin and cultured fibroblasts of two patients with Ullrich's disease with collagen VI deficiency, and speculated that an abnormality of cell adhesion may be involved in the pathogenesis of the disease.]. 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:16258947
;
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:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}