@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP285786.RAbFquRuqDGg5_UIOHt2V5TkRhQ1WJLyjrMHZF27zoptM
> .
@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:NP285786.RAbFquRuqDGg5_UIOHt2V5TkRhQ1WJLyjrMHZF27zoptM130_head
{
this:
np:hasAssertion
dgn-np:NP285786.RAbFquRuqDGg5_UIOHt2V5TkRhQ1WJLyjrMHZF27zoptM130_assertion
;
np:hasProvenance
dgn-np:NP285786.RAbFquRuqDGg5_UIOHt2V5TkRhQ1WJLyjrMHZF27zoptM130_provenance
;
np:hasPublicationInfo
dgn-np:NP285786.RAbFquRuqDGg5_UIOHt2V5TkRhQ1WJLyjrMHZF27zoptM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP285786.RAbFquRuqDGg5_UIOHt2V5TkRhQ1WJLyjrMHZF27zoptM130_assertion
a
np:Assertion
.
dgn-np:NP285786.RAbFquRuqDGg5_UIOHt2V5TkRhQ1WJLyjrMHZF27zoptM130_provenance
a
np:Provenance
.
dgn-np:NP285786.RAbFquRuqDGg5_UIOHt2V5TkRhQ1WJLyjrMHZF27zoptM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP285786.RAbFquRuqDGg5_UIOHt2V5TkRhQ1WJLyjrMHZF27zoptM130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0677886
a
ncit:C7057
.
dgn-gda:DGN9aa8b2fca15c501220c5731b3292d11e
sio:SIO_000628
miriam-gene:672
,
lld:C0677886
;
a
sio:SIO_001121
.
}
dgn-np:NP285786.RAbFquRuqDGg5_UIOHt2V5TkRhQ1WJLyjrMHZF27zoptM130_provenance
{
dgn-np:NP285786.RAbFquRuqDGg5_UIOHt2V5TkRhQ1WJLyjrMHZF27zoptM130_assertion
dcterms:description
"[Ninety-four patients with epithelial ovarian cancer and available snap-frozen tissue were screened for BRCA1 mutations by both PTT (five individual PCR reactions with complete translation of the product in the TNT System (Promega, Madison, WI)) and SSCP (41 individual PCR reactions covering the entire coding sequence).]. 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:11668617
;
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:NP285786.RAbFquRuqDGg5_UIOHt2V5TkRhQ1WJLyjrMHZF27zoptM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:41+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" .
}