@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_head
{
this:
np:hasAssertion
dgn-np:NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_assertion
;
np:hasProvenance
dgn-np:NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_provenance
;
np:hasPublicationInfo
dgn-np:NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_assertion
a
np:Assertion
.
dgn-np:NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_provenance
a
np:Provenance
.
dgn-np:NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_assertion
{
miriam-gene:1836
a
ncit:C16612
.
lld:C0026760
a
ncit:C7057
.
dgn-gda:DGNfe681269d18cb3d0b19a710fca147a84
sio:SIO_000628
miriam-gene:1836
,
lld:C0026760
;
a
sio:SIO_001121
.
}
dgn-np:NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_provenance
{
dgn-np:NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_assertion
dcterms:description
"[The results show that mutations in COL9A1 can cause MED, but they also suggest that mutations in COL9A1, COL9A2, COL9A3, COMP, and DTDST are not the major causes of MED and that there exists at least one additional locus.]. 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:11565064
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:15+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}