@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k
> .
@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:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_head
{
this:
np:hasAssertion
dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_assertion
;
np:hasProvenance
dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_provenance
;
np:hasPublicationInfo
dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_assertion
a
np:Assertion
.
dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_provenance
a
np:Provenance
.
dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C1336076
a
ncit:C7057
.
dgn-gda:DGNdd83531c2a97e457625f4778e4d2fa8a
sio:SIO_000628
miriam-gene:675
,
lld:C1336076
;
a
sio:SIO_001121
.
}
dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_provenance
{
dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_assertion
dcterms:description
"[Certain frequently mutated exons such as 2, 5, 11, 13 and 20 of BRCA1, exons 2, 9, 11 (for 6174delT), 18 and 20 of BRCA2 and 4-9 exons of p53 gene were analyzed in sporadic breast cancer while all 22 coding exons of BRCA1 including its flanking intronic regions along with above mentioned exons of BRCA2 and p53 gene were analyzed in familial breast cancer patients.]. 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:15564800
;
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:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:57+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" .
}