@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP552657.RA3YIkNjUg4R3agSsNVRDHuf51hoPqC4G2ac2k4Z8Gtck
> .
@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:NP552657.RA3YIkNjUg4R3agSsNVRDHuf51hoPqC4G2ac2k4Z8Gtck130_head
{
this:
np:hasAssertion
dgn-np:NP552657.RA3YIkNjUg4R3agSsNVRDHuf51hoPqC4G2ac2k4Z8Gtck130_assertion
;
np:hasProvenance
dgn-np:NP552657.RA3YIkNjUg4R3agSsNVRDHuf51hoPqC4G2ac2k4Z8Gtck130_provenance
;
np:hasPublicationInfo
dgn-np:NP552657.RA3YIkNjUg4R3agSsNVRDHuf51hoPqC4G2ac2k4Z8Gtck130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP552657.RA3YIkNjUg4R3agSsNVRDHuf51hoPqC4G2ac2k4Z8Gtck130_assertion
a
np:Assertion
.
dgn-np:NP552657.RA3YIkNjUg4R3agSsNVRDHuf51hoPqC4G2ac2k4Z8Gtck130_provenance
a
np:Provenance
.
dgn-np:NP552657.RA3YIkNjUg4R3agSsNVRDHuf51hoPqC4G2ac2k4Z8Gtck130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP552657.RA3YIkNjUg4R3agSsNVRDHuf51hoPqC4G2ac2k4Z8Gtck130_assertion
{
miriam-gene:2335
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGNebf868a9996a307b02ea8a22461909af
sio:SIO_000628
miriam-gene:2335
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP552657.RA3YIkNjUg4R3agSsNVRDHuf51hoPqC4G2ac2k4Z8Gtck130_provenance
{
dgn-np:NP552657.RA3YIkNjUg4R3agSsNVRDHuf51hoPqC4G2ac2k4Z8Gtck130_assertion
dcterms:description
"[Therefore, the much increased expression of oncofetal fibronectin mRNA in these carcinomas is not caused by the alternation in splicing, but may be caused by an increase in promoter activity or stability of mRNA of the fibronectin gene.]. 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:10090132
;
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:NP552657.RA3YIkNjUg4R3agSsNVRDHuf51hoPqC4G2ac2k4Z8Gtck130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:33+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" .
}