@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP587894.RAiwe7yAUopbHq_qR-kF7b5rGCkIBqtLgtigM-wgz8llM
> .
@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:NP587894.RAiwe7yAUopbHq_qR-kF7b5rGCkIBqtLgtigM-wgz8llM130_head
{
this:
np:hasAssertion
dgn-np:NP587894.RAiwe7yAUopbHq_qR-kF7b5rGCkIBqtLgtigM-wgz8llM130_assertion
;
np:hasProvenance
dgn-np:NP587894.RAiwe7yAUopbHq_qR-kF7b5rGCkIBqtLgtigM-wgz8llM130_provenance
;
np:hasPublicationInfo
dgn-np:NP587894.RAiwe7yAUopbHq_qR-kF7b5rGCkIBqtLgtigM-wgz8llM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP587894.RAiwe7yAUopbHq_qR-kF7b5rGCkIBqtLgtigM-wgz8llM130_assertion
a
np:Assertion
.
dgn-np:NP587894.RAiwe7yAUopbHq_qR-kF7b5rGCkIBqtLgtigM-wgz8llM130_provenance
a
np:Provenance
.
dgn-np:NP587894.RAiwe7yAUopbHq_qR-kF7b5rGCkIBqtLgtigM-wgz8llM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP587894.RAiwe7yAUopbHq_qR-kF7b5rGCkIBqtLgtigM-wgz8llM130_assertion
{
miriam-gene:146
a
ncit:C16612
.
lld:C0086437
a
ncit:C7057
.
dgn-gda:DGN30bb561fe065853d15356b4645ed71a9
sio:SIO_000628
miriam-gene:146
,
lld:C0086437
;
a
sio:SIO_001121
.
}
dgn-np:NP587894.RAiwe7yAUopbHq_qR-kF7b5rGCkIBqtLgtigM-wgz8llM130_provenance
{
dgn-np:NP587894.RAiwe7yAUopbHq_qR-kF7b5rGCkIBqtLgtigM-wgz8llM130_assertion
dcterms:description
"[This distribution, and the association of alpha1(V), alpha2(V), and alpha3(V) chains in heterotrimers, suggests the human alpha3(V) gene COL5A3 as a candidate locus for at least some cases of classical EDS in which the alpha1(V) and alpha2(V) genes have been excluded, and for at least some cases of the hypermobility type of EDS, a condition marked by gross joint laxity and chronic musculoskeletal pain.]. 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:10722718
;
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:NP587894.RAiwe7yAUopbHq_qR-kF7b5rGCkIBqtLgtigM-wgz8llM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:54+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" .
}