@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP443990.RAqazUVC7r2GcFOF09sz0NH6w1az-rcRNmIw-qN9qsACM
> .
@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:NP443990.RAqazUVC7r2GcFOF09sz0NH6w1az-rcRNmIw-qN9qsACM130_head
{
this:
np:hasAssertion
dgn-np:NP443990.RAqazUVC7r2GcFOF09sz0NH6w1az-rcRNmIw-qN9qsACM130_assertion
;
np:hasProvenance
dgn-np:NP443990.RAqazUVC7r2GcFOF09sz0NH6w1az-rcRNmIw-qN9qsACM130_provenance
;
np:hasPublicationInfo
dgn-np:NP443990.RAqazUVC7r2GcFOF09sz0NH6w1az-rcRNmIw-qN9qsACM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP443990.RAqazUVC7r2GcFOF09sz0NH6w1az-rcRNmIw-qN9qsACM130_assertion
a
np:Assertion
.
dgn-np:NP443990.RAqazUVC7r2GcFOF09sz0NH6w1az-rcRNmIw-qN9qsACM130_provenance
a
np:Provenance
.
dgn-np:NP443990.RAqazUVC7r2GcFOF09sz0NH6w1az-rcRNmIw-qN9qsACM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP443990.RAqazUVC7r2GcFOF09sz0NH6w1az-rcRNmIw-qN9qsACM130_assertion
{
miriam-gene:2335
a
ncit:C16612
.
lld:C0585442
a
ncit:C7057
.
dgn-gda:DGN7d450b38239c87136dc46b47db08245c
sio:SIO_000628
miriam-gene:2335
,
lld:C0585442
;
a
sio:SIO_001121
.
}
dgn-np:NP443990.RAqazUVC7r2GcFOF09sz0NH6w1az-rcRNmIw-qN9qsACM130_provenance
{
dgn-np:NP443990.RAqazUVC7r2GcFOF09sz0NH6w1az-rcRNmIw-qN9qsACM130_assertion
dcterms:description
"[The aim of this study was to investigate the expression pattern of fibronectin splice variants in bone cell lines and in different human bone tissue samples (mature bone, early stages of fracture healing, hypotrophic nonunion, osteosarcoma).]. 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:15589214
;
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:NP443990.RAqazUVC7r2GcFOF09sz0NH6w1az-rcRNmIw-qN9qsACM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:24+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" .
}