@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP267682.RA3G3NsBaNkRC3j6aMOo8An5qQZihahKQm3EzswBnOpU8
> .
@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:NP267682.RA3G3NsBaNkRC3j6aMOo8An5qQZihahKQm3EzswBnOpU8130_head
{
this:
np:hasAssertion
dgn-np:NP267682.RA3G3NsBaNkRC3j6aMOo8An5qQZihahKQm3EzswBnOpU8130_assertion
;
np:hasProvenance
dgn-np:NP267682.RA3G3NsBaNkRC3j6aMOo8An5qQZihahKQm3EzswBnOpU8130_provenance
;
np:hasPublicationInfo
dgn-np:NP267682.RA3G3NsBaNkRC3j6aMOo8An5qQZihahKQm3EzswBnOpU8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP267682.RA3G3NsBaNkRC3j6aMOo8An5qQZihahKQm3EzswBnOpU8130_assertion
a
np:Assertion
.
dgn-np:NP267682.RA3G3NsBaNkRC3j6aMOo8An5qQZihahKQm3EzswBnOpU8130_provenance
a
np:Provenance
.
dgn-np:NP267682.RA3G3NsBaNkRC3j6aMOo8An5qQZihahKQm3EzswBnOpU8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP267682.RA3G3NsBaNkRC3j6aMOo8An5qQZihahKQm3EzswBnOpU8130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNad1a5d5c5f280878d60fc2a73cadf982
sio:SIO_000628
miriam-gene:7428
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP267682.RA3G3NsBaNkRC3j6aMOo8An5qQZihahKQm3EzswBnOpU8130_provenance
{
dgn-np:NP267682.RA3G3NsBaNkRC3j6aMOo8An5qQZihahKQm3EzswBnOpU8130_assertion
dcterms:description
"[Thanks to the flexible structure of the UMD software, it has been successfully adapted to nine genes either involved in cancer (APC, P53, RB1, MEN1, SUR1, VHL, and WT1) or in genetic diseases (FBN1 and LDLR).]. 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:10612827
;
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:NP267682.RA3G3NsBaNkRC3j6aMOo8An5qQZihahKQm3EzswBnOpU8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:29+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" .
}