@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y
> .
@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:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_head
{
this:
np:hasAssertion
dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_assertion
;
np:hasProvenance
dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_assertion
a
np:Assertion
.
dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_provenance
a
np:Provenance
.
dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_assertion
{
miriam-gene:2335
a
ncit:C16612
.
lld:C0410179
a
ncit:C7057
.
dgn-gda:DGNbfffe5af09e4d9528a100ac8afba22d4
sio:SIO_000628
miriam-gene:2335
,
lld:C0410179
;
a
sio:SIO_001121
.
}
dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_provenance
{
dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_assertion
dcterms:description
"[These results suggest that collagen VI deficiency may lead to the reduction of fibronectin receptors and that an abnormality of cell adhesion may be involved in the pathogenesis of Ullrich's 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:12402292
;
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:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:04+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" .
}