@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP355902.RAWMB0xG-c58nz4VzN37inIA5EW-JhzJMZ4BRPQUqpELA
> .
@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:NP355902.RAWMB0xG-c58nz4VzN37inIA5EW-JhzJMZ4BRPQUqpELA130_head
{
this:
np:hasAssertion
dgn-np:NP355902.RAWMB0xG-c58nz4VzN37inIA5EW-JhzJMZ4BRPQUqpELA130_assertion
;
np:hasProvenance
dgn-np:NP355902.RAWMB0xG-c58nz4VzN37inIA5EW-JhzJMZ4BRPQUqpELA130_provenance
;
np:hasPublicationInfo
dgn-np:NP355902.RAWMB0xG-c58nz4VzN37inIA5EW-JhzJMZ4BRPQUqpELA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP355902.RAWMB0xG-c58nz4VzN37inIA5EW-JhzJMZ4BRPQUqpELA130_assertion
a
np:Assertion
.
dgn-np:NP355902.RAWMB0xG-c58nz4VzN37inIA5EW-JhzJMZ4BRPQUqpELA130_provenance
a
np:Provenance
.
dgn-np:NP355902.RAWMB0xG-c58nz4VzN37inIA5EW-JhzJMZ4BRPQUqpELA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP355902.RAWMB0xG-c58nz4VzN37inIA5EW-JhzJMZ4BRPQUqpELA130_assertion
{
miriam-gene:2189
a
ncit:C16612
.
lld:C0030297
a
ncit:C7057
.
dgn-gda:DGNa82d336dc6d16dedff5639be2de60b21
sio:SIO_000628
miriam-gene:2189
,
lld:C0030297
;
a
sio:SIO_001121
.
}
dgn-np:NP355902.RAWMB0xG-c58nz4VzN37inIA5EW-JhzJMZ4BRPQUqpELA130_provenance
{
dgn-np:NP355902.RAWMB0xG-c58nz4VzN37inIA5EW-JhzJMZ4BRPQUqpELA130_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:NP355902.RAWMB0xG-c58nz4VzN37inIA5EW-JhzJMZ4BRPQUqpELA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:29+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" .
}