@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP396397.RAZMw_ddvfIV9MuQpm4N9O6WCWJG74cnNg6hC6Ki5zTXM
> .
@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:NP396397.RAZMw_ddvfIV9MuQpm4N9O6WCWJG74cnNg6hC6Ki5zTXM130_head
{
this:
np:hasAssertion
dgn-np:NP396397.RAZMw_ddvfIV9MuQpm4N9O6WCWJG74cnNg6hC6Ki5zTXM130_assertion
;
np:hasProvenance
dgn-np:NP396397.RAZMw_ddvfIV9MuQpm4N9O6WCWJG74cnNg6hC6Ki5zTXM130_provenance
;
np:hasPublicationInfo
dgn-np:NP396397.RAZMw_ddvfIV9MuQpm4N9O6WCWJG74cnNg6hC6Ki5zTXM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP396397.RAZMw_ddvfIV9MuQpm4N9O6WCWJG74cnNg6hC6Ki5zTXM130_assertion
a
np:Assertion
.
dgn-np:NP396397.RAZMw_ddvfIV9MuQpm4N9O6WCWJG74cnNg6hC6Ki5zTXM130_provenance
a
np:Provenance
.
dgn-np:NP396397.RAZMw_ddvfIV9MuQpm4N9O6WCWJG74cnNg6hC6Ki5zTXM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP396397.RAZMw_ddvfIV9MuQpm4N9O6WCWJG74cnNg6hC6Ki5zTXM130_assertion
{
miriam-gene:51151
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN0526b6481ab46a71cf1ac6b98ea36e2a
sio:SIO_000628
miriam-gene:51151
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP396397.RAZMw_ddvfIV9MuQpm4N9O6WCWJG74cnNg6hC6Ki5zTXM130_provenance
{
dgn-np:NP396397.RAZMw_ddvfIV9MuQpm4N9O6WCWJG74cnNg6hC6Ki5zTXM130_assertion
dcterms:description
"[For the most part, these SNPs are fairly uncommon in the population, but some, most notably for SULT isoform 1A1, are commonly found and have been associated with cancer risk for a variety of tumor sites and also with response to therapeutic agents.]. 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:16550167
;
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:NP396397.RAZMw_ddvfIV9MuQpm4N9O6WCWJG74cnNg6hC6Ki5zTXM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:56+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" .
}