@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc
> .
@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:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_head
{
this:
np:hasAssertion
dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_assertion
;
np:hasProvenance
dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_provenance
;
np:hasPublicationInfo
dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_assertion
a
np:Assertion
.
dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_provenance
a
np:Provenance
.
dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_assertion
{
miriam-gene:49
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN97fe64cc30eec0374f569a8353ae7b72
sio:SIO_000628
miriam-gene:49
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_provenance
{
dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_assertion
dcterms:description
"[A total of 57 different strains (33 from patients and 24 from healthy members of ACR families not at an increased risk for colon polyposis) were tested for their frequencies of spontaneous structural chromosome aberrations, i.e., chromatid and isochromatid gaps, breaks, and interchanges.]. 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:4016717
;
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:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:51+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" .
}