@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP686924.RAQxolyI8JPNKMCr-y0On8yEEeM3rkgpN5Qc0u7RsraTc
> .
@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:NP686924.RAQxolyI8JPNKMCr-y0On8yEEeM3rkgpN5Qc0u7RsraTc130_head
{
this:
np:hasAssertion
dgn-np:NP686924.RAQxolyI8JPNKMCr-y0On8yEEeM3rkgpN5Qc0u7RsraTc130_assertion
;
np:hasProvenance
dgn-np:NP686924.RAQxolyI8JPNKMCr-y0On8yEEeM3rkgpN5Qc0u7RsraTc130_provenance
;
np:hasPublicationInfo
dgn-np:NP686924.RAQxolyI8JPNKMCr-y0On8yEEeM3rkgpN5Qc0u7RsraTc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP686924.RAQxolyI8JPNKMCr-y0On8yEEeM3rkgpN5Qc0u7RsraTc130_assertion
a
np:Assertion
.
dgn-np:NP686924.RAQxolyI8JPNKMCr-y0On8yEEeM3rkgpN5Qc0u7RsraTc130_provenance
a
np:Provenance
.
dgn-np:NP686924.RAQxolyI8JPNKMCr-y0On8yEEeM3rkgpN5Qc0u7RsraTc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP686924.RAQxolyI8JPNKMCr-y0On8yEEeM3rkgpN5Qc0u7RsraTc130_assertion
{
miriam-gene:2335
a
ncit:C16612
.
lld:C0027819
a
ncit:C7057
.
dgn-gda:DGN8ca0a308c2c0d5db834f81a109750612
sio:SIO_000628
miriam-gene:2335
,
lld:C0027819
;
a
sio:SIO_001121
.
}
dgn-np:NP686924.RAQxolyI8JPNKMCr-y0On8yEEeM3rkgpN5Qc0u7RsraTc130_provenance
{
dgn-np:NP686924.RAQxolyI8JPNKMCr-y0On8yEEeM3rkgpN5Qc0u7RsraTc130_assertion
dcterms:description
"[We report the effect of the stable expression of a 13 amino acid human fibronectin (FN) peptide (FN13) on the organization of the FN extracellular matrix (ECM) and of FN integrin receptors (FNRs), in relationship with the inhibition of cellular invasion, in three FN-ECM defective human tumor-derived cell lines: SK-Hep1C3, hepatoma, ACN, neuroblastoma, and SK-OV-3, ovary carcinoma.]. 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:17383746
;
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:NP686924.RAQxolyI8JPNKMCr-y0On8yEEeM3rkgpN5Qc0u7RsraTc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:57+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" .
}