@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP331077.RAzO3pjLUKWspOm0yL1H6-kufFVRv0ot-n6UNHvtvVL40
> .
@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:NP331077.RAzO3pjLUKWspOm0yL1H6-kufFVRv0ot-n6UNHvtvVL40130_head
{
this:
np:hasAssertion
dgn-np:NP331077.RAzO3pjLUKWspOm0yL1H6-kufFVRv0ot-n6UNHvtvVL40130_assertion
;
np:hasProvenance
dgn-np:NP331077.RAzO3pjLUKWspOm0yL1H6-kufFVRv0ot-n6UNHvtvVL40130_provenance
;
np:hasPublicationInfo
dgn-np:NP331077.RAzO3pjLUKWspOm0yL1H6-kufFVRv0ot-n6UNHvtvVL40130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP331077.RAzO3pjLUKWspOm0yL1H6-kufFVRv0ot-n6UNHvtvVL40130_assertion
a
np:Assertion
.
dgn-np:NP331077.RAzO3pjLUKWspOm0yL1H6-kufFVRv0ot-n6UNHvtvVL40130_provenance
a
np:Provenance
.
dgn-np:NP331077.RAzO3pjLUKWspOm0yL1H6-kufFVRv0ot-n6UNHvtvVL40130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP331077.RAzO3pjLUKWspOm0yL1H6-kufFVRv0ot-n6UNHvtvVL40130_assertion
{
miriam-gene:1299
a
ncit:C16612
.
lld:C0410538
a
ncit:C7057
.
dgn-gda:DGNcf20aeefa7e322da178ab905c3fbc968
sio:SIO_000628
miriam-gene:1299
,
lld:C0410538
;
a
sio:SIO_001121
.
}
dgn-np:NP331077.RAzO3pjLUKWspOm0yL1H6-kufFVRv0ot-n6UNHvtvVL40130_provenance
{
dgn-np:NP331077.RAzO3pjLUKWspOm0yL1H6-kufFVRv0ot-n6UNHvtvVL40130_assertion
dcterms:description
"[MED, and PSACH mutations, despite displaying phenotypic differences, demonstrated only subtle differences in their cellular viability and mRNA and protein expression of components of the extracellular matrix, including those that interact with COMP.]. 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:20578249
;
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:NP331077.RAzO3pjLUKWspOm0yL1H6-kufFVRv0ot-n6UNHvtvVL40130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:15+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: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" .
}