@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP501467.RAY7Ygk_TICD-u9Q83ValDuU039UyWgtR40-LcmDCekG8
> .
@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:NP501467.RAY7Ygk_TICD-u9Q83ValDuU039UyWgtR40-LcmDCekG8130_head
{
this:
np:hasAssertion
dgn-np:NP501467.RAY7Ygk_TICD-u9Q83ValDuU039UyWgtR40-LcmDCekG8130_assertion
;
np:hasProvenance
dgn-np:NP501467.RAY7Ygk_TICD-u9Q83ValDuU039UyWgtR40-LcmDCekG8130_provenance
;
np:hasPublicationInfo
dgn-np:NP501467.RAY7Ygk_TICD-u9Q83ValDuU039UyWgtR40-LcmDCekG8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP501467.RAY7Ygk_TICD-u9Q83ValDuU039UyWgtR40-LcmDCekG8130_assertion
a
np:Assertion
.
dgn-np:NP501467.RAY7Ygk_TICD-u9Q83ValDuU039UyWgtR40-LcmDCekG8130_provenance
a
np:Provenance
.
dgn-np:NP501467.RAY7Ygk_TICD-u9Q83ValDuU039UyWgtR40-LcmDCekG8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP501467.RAY7Ygk_TICD-u9Q83ValDuU039UyWgtR40-LcmDCekG8130_assertion
{
miriam-gene:146
a
ncit:C16612
.
lld:C0013720
a
ncit:C7057
.
dgn-gda:DGNa68c66f3848c49e43ab003d057d48c1c
sio:SIO_000628
miriam-gene:146
,
lld:C0013720
;
a
sio:SIO_001121
.
}
dgn-np:NP501467.RAY7Ygk_TICD-u9Q83ValDuU039UyWgtR40-LcmDCekG8130_provenance
{
dgn-np:NP501467.RAY7Ygk_TICD-u9Q83ValDuU039UyWgtR40-LcmDCekG8130_assertion
dcterms:description
"[The low abundance fibrillar collagen type V is widely distributed in tissues as an alpha1(V)(2)alpha2(V) heterotrimer that helps regulate the diameters of fibrils of the abundant collagen type I. Mutations in the alpha1(V) and alpha2(V) chain genes have been identified in some cases of classical Ehlers-Danlos syndrome (EDS), in which aberrant collagen fibrils are associated with connective tissue fragility, particularly in skin and joints.]. 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:NP501467.RAY7Ygk_TICD-u9Q83ValDuU039UyWgtR40-LcmDCekG8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:59+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" .
}