@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw
> .
@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:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_head
{
this:
np:hasAssertion
dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_assertion
;
np:hasProvenance
dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_provenance
;
np:hasPublicationInfo
dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_assertion
a
np:Assertion
.
dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_provenance
a
np:Provenance
.
dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_assertion
{
miriam-gene:2176
a
ncit:C16612
.
lld:C0030297
a
ncit:C7057
.
dgn-gda:DGNe4c85ec15cc4550a7c052dcf793397dd
sio:SIO_000628
miriam-gene:2176
,
lld:C0030297
;
a
sio:SIO_001121
.
}
dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_provenance
{
dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_assertion
dcterms:description
"[Sequence analysis of 38 individuals with familial pancreatic cancer enrolled in the National Familial Pancreatic Tumor Registry (NFPTR) revealed previously identified polymorphisms within two exons and one intron of FANCC, and in three introns of FANCG.]. 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:14726700
;
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:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:52+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" .
}