@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP792850.RASpavJQ7caYO3e62VQg0DGmMMXVE5T19HWz8CxNrihtw
> .
@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:NP792850.RASpavJQ7caYO3e62VQg0DGmMMXVE5T19HWz8CxNrihtw130_head
{
this:
np:hasAssertion
dgn-np:NP792850.RASpavJQ7caYO3e62VQg0DGmMMXVE5T19HWz8CxNrihtw130_assertion
;
np:hasProvenance
dgn-np:NP792850.RASpavJQ7caYO3e62VQg0DGmMMXVE5T19HWz8CxNrihtw130_provenance
;
np:hasPublicationInfo
dgn-np:NP792850.RASpavJQ7caYO3e62VQg0DGmMMXVE5T19HWz8CxNrihtw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP792850.RASpavJQ7caYO3e62VQg0DGmMMXVE5T19HWz8CxNrihtw130_assertion
a
np:Assertion
.
dgn-np:NP792850.RASpavJQ7caYO3e62VQg0DGmMMXVE5T19HWz8CxNrihtw130_provenance
a
np:Provenance
.
dgn-np:NP792850.RASpavJQ7caYO3e62VQg0DGmMMXVE5T19HWz8CxNrihtw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP792850.RASpavJQ7caYO3e62VQg0DGmMMXVE5T19HWz8CxNrihtw130_assertion
{
miriam-gene:10522
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN2fe642653dd7d179296a583ad024ae04
sio:SIO_000628
miriam-gene:10522
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP792850.RASpavJQ7caYO3e62VQg0DGmMMXVE5T19HWz8CxNrihtw130_provenance
{
dgn-np:NP792850.RASpavJQ7caYO3e62VQg0DGmMMXVE5T19HWz8CxNrihtw130_assertion
dcterms:description
"[This is the first report of genetic alterations in the spn gene in a human malignancy and suggests that genetic alterations in spn and the resulting immunohistochemical phenotypes based on SPN subcellular localization in CRCs may be useful in determining prognosis of patients with subtypes of CRC.]. 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:11705868
;
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:NP792850.RASpavJQ7caYO3e62VQg0DGmMMXVE5T19HWz8CxNrihtw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:07+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" .
}