@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP554980.RALyVHq13cEMyIFycYfwgWH6BC7FGfOFMeYuzXfcba4HU
> .
@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:NP554980.RALyVHq13cEMyIFycYfwgWH6BC7FGfOFMeYuzXfcba4HU130_head
{
this:
np:hasAssertion
dgn-np:NP554980.RALyVHq13cEMyIFycYfwgWH6BC7FGfOFMeYuzXfcba4HU130_assertion
;
np:hasProvenance
dgn-np:NP554980.RALyVHq13cEMyIFycYfwgWH6BC7FGfOFMeYuzXfcba4HU130_provenance
;
np:hasPublicationInfo
dgn-np:NP554980.RALyVHq13cEMyIFycYfwgWH6BC7FGfOFMeYuzXfcba4HU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP554980.RALyVHq13cEMyIFycYfwgWH6BC7FGfOFMeYuzXfcba4HU130_assertion
a
np:Assertion
.
dgn-np:NP554980.RALyVHq13cEMyIFycYfwgWH6BC7FGfOFMeYuzXfcba4HU130_provenance
a
np:Provenance
.
dgn-np:NP554980.RALyVHq13cEMyIFycYfwgWH6BC7FGfOFMeYuzXfcba4HU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP554980.RALyVHq13cEMyIFycYfwgWH6BC7FGfOFMeYuzXfcba4HU130_assertion
{
miriam-gene:2189
a
ncit:C16612
.
lld:C0030297
a
ncit:C7057
.
dgn-gda:DGNda16218d0cf0d85662c0343b335f29e7
sio:SIO_000628
miriam-gene:2189
,
lld:C0030297
;
a
sio:SIO_001121
.
}
dgn-np:NP554980.RALyVHq13cEMyIFycYfwgWH6BC7FGfOFMeYuzXfcba4HU130_provenance
{
dgn-np:NP554980.RALyVHq13cEMyIFycYfwgWH6BC7FGfOFMeYuzXfcba4HU130_assertion
dcterms:description
"[The recent identification of FANCC and FANCG mutations in resected pancreatic tumors selected for loss of heterozygosity on chromosome 9, some of which were present in the germ line DNA, suggests that inactivation of these and other Fanconi complementation group genes may contribute to pancreatic cancer.]. 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:15695377
;
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:NP554980.RALyVHq13cEMyIFycYfwgWH6BC7FGfOFMeYuzXfcba4HU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:34+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" .
}