@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP428285.RA1kwYb8wcCv67d5Zji5tC5_tQegFNU7tkm9cdx4vDn_k
> .
@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:NP428285.RA1kwYb8wcCv67d5Zji5tC5_tQegFNU7tkm9cdx4vDn_k130_head
{
this:
np:hasAssertion
dgn-np:NP428285.RA1kwYb8wcCv67d5Zji5tC5_tQegFNU7tkm9cdx4vDn_k130_assertion
;
np:hasProvenance
dgn-np:NP428285.RA1kwYb8wcCv67d5Zji5tC5_tQegFNU7tkm9cdx4vDn_k130_provenance
;
np:hasPublicationInfo
dgn-np:NP428285.RA1kwYb8wcCv67d5Zji5tC5_tQegFNU7tkm9cdx4vDn_k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP428285.RA1kwYb8wcCv67d5Zji5tC5_tQegFNU7tkm9cdx4vDn_k130_assertion
a
np:Assertion
.
dgn-np:NP428285.RA1kwYb8wcCv67d5Zji5tC5_tQegFNU7tkm9cdx4vDn_k130_provenance
a
np:Provenance
.
dgn-np:NP428285.RA1kwYb8wcCv67d5Zji5tC5_tQegFNU7tkm9cdx4vDn_k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP428285.RA1kwYb8wcCv67d5Zji5tC5_tQegFNU7tkm9cdx4vDn_k130_assertion
{
miriam-gene:1311
a
ncit:C16612
.
lld:C0007302
a
ncit:C7057
.
dgn-gda:DGN2b94fd35144b372de1d251cbe03c64db
sio:SIO_000628
miriam-gene:1311
,
lld:C0007302
;
a
sio:SIO_001121
.
}
dgn-np:NP428285.RA1kwYb8wcCv67d5Zji5tC5_tQegFNU7tkm9cdx4vDn_k130_provenance
{
dgn-np:NP428285.RA1kwYb8wcCv67d5Zji5tC5_tQegFNU7tkm9cdx4vDn_k130_assertion
dcterms:description
"[Studies in chondrocytes and cartilage biopsies suggest that the cartilage disease is caused by retention of mutant COMP in the endoplasmic reticulum of chondrocytes and by disruption of the collagen network of the extracellular matrix.]. 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:17307347
;
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:NP428285.RA1kwYb8wcCv67d5Zji5tC5_tQegFNU7tkm9cdx4vDn_k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:14+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" .
}