@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP471592.RAVsKHclbBqYbFUFTYNc1jeWx6m1gNTXcJD0fkfJDvVHg
> .
@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:NP471592.RAVsKHclbBqYbFUFTYNc1jeWx6m1gNTXcJD0fkfJDvVHg130_head
{
this:
np:hasAssertion
dgn-np:NP471592.RAVsKHclbBqYbFUFTYNc1jeWx6m1gNTXcJD0fkfJDvVHg130_assertion
;
np:hasProvenance
dgn-np:NP471592.RAVsKHclbBqYbFUFTYNc1jeWx6m1gNTXcJD0fkfJDvVHg130_provenance
;
np:hasPublicationInfo
dgn-np:NP471592.RAVsKHclbBqYbFUFTYNc1jeWx6m1gNTXcJD0fkfJDvVHg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP471592.RAVsKHclbBqYbFUFTYNc1jeWx6m1gNTXcJD0fkfJDvVHg130_assertion
a
np:Assertion
.
dgn-np:NP471592.RAVsKHclbBqYbFUFTYNc1jeWx6m1gNTXcJD0fkfJDvVHg130_provenance
a
np:Provenance
.
dgn-np:NP471592.RAVsKHclbBqYbFUFTYNc1jeWx6m1gNTXcJD0fkfJDvVHg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP471592.RAVsKHclbBqYbFUFTYNc1jeWx6m1gNTXcJD0fkfJDvVHg130_assertion
{
miriam-gene:2335
a
ncit:C16612
.
lld:C0027627
a
ncit:C7057
.
dgn-gda:DGNce2124b2e473e8875484126806231b02
sio:SIO_000628
miriam-gene:2335
,
lld:C0027627
;
a
sio:SIO_001121
.
}
dgn-np:NP471592.RAVsKHclbBqYbFUFTYNc1jeWx6m1gNTXcJD0fkfJDvVHg130_provenance
{
dgn-np:NP471592.RAVsKHclbBqYbFUFTYNc1jeWx6m1gNTXcJD0fkfJDvVHg130_assertion
dcterms:description
"[Additional experiments using cell lines stably expressing the mutated FN cDNA demonstrated that the point mutation in FN was responsible for the loss of FN staining in extracellular matrices and the enhancement of tumor cell migration.]. 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:12045238
;
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:NP471592.RAVsKHclbBqYbFUFTYNc1jeWx6m1gNTXcJD0fkfJDvVHg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:42+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" .
}