@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP676021.RAYGzLdz64Ia26ZYGrzBw9TxYttRI7maArNsJHinXrUNI
> .
@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:NP676021.RAYGzLdz64Ia26ZYGrzBw9TxYttRI7maArNsJHinXrUNI130_head
{
this:
np:hasAssertion
dgn-np:NP676021.RAYGzLdz64Ia26ZYGrzBw9TxYttRI7maArNsJHinXrUNI130_assertion
;
np:hasProvenance
dgn-np:NP676021.RAYGzLdz64Ia26ZYGrzBw9TxYttRI7maArNsJHinXrUNI130_provenance
;
np:hasPublicationInfo
dgn-np:NP676021.RAYGzLdz64Ia26ZYGrzBw9TxYttRI7maArNsJHinXrUNI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP676021.RAYGzLdz64Ia26ZYGrzBw9TxYttRI7maArNsJHinXrUNI130_assertion
a
np:Assertion
.
dgn-np:NP676021.RAYGzLdz64Ia26ZYGrzBw9TxYttRI7maArNsJHinXrUNI130_provenance
a
np:Provenance
.
dgn-np:NP676021.RAYGzLdz64Ia26ZYGrzBw9TxYttRI7maArNsJHinXrUNI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP676021.RAYGzLdz64Ia26ZYGrzBw9TxYttRI7maArNsJHinXrUNI130_assertion
{
miriam-gene:58189
a
ncit:C16612
.
lld:C0027708
a
ncit:C7057
.
dgn-gda:DGN2371a097cb44dd41991e3abf56cece7c
sio:SIO_000628
miriam-gene:58189
,
lld:C0027708
;
a
sio:SIO_001121
.
}
dgn-np:NP676021.RAYGzLdz64Ia26ZYGrzBw9TxYttRI7maArNsJHinXrUNI130_provenance
{
dgn-np:NP676021.RAYGzLdz64Ia26ZYGrzBw9TxYttRI7maArNsJHinXrUNI130_assertion
dcterms:description
"[The WFDC1 gene was mapped by FISH analysis to human Chromosome (Chr) 16q24, an area of frequent loss of heterozygosity (LOH) previously identified in multiple cancers including prostate, breast, hepatocellular, and Wilms' tumor.]. 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:10967136
;
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:NP676021.RAYGzLdz64Ia26ZYGrzBw9TxYttRI7maArNsJHinXrUNI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:48+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" .
}