@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_head
{
this:
np:hasAssertion
dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_assertion
;
np:hasProvenance
dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_provenance
;
np:hasPublicationInfo
dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_assertion
a
np:Assertion
.
dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_provenance
a
np:Provenance
.
dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_assertion
{
miriam-gene:28471
a
ncit:C16612
.
lld:C0206664
a
ncit:C7057
.
dgn-gda:DGN3a80350ad4d9d8f9280f6567af9f9b89
sio:SIO_000628
miriam-gene:28471
,
lld:C0206664
;
a
sio:SIO_001121
.
}
dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_provenance
{
dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_assertion
dcterms:description
"[We examined eight human germ cell cancer lines (GCCLs) for cytogenetic abnormalities and found an isochromosome 12p, i(12p), marker in all seven male nonseminoma GCCLs, but not in the single female teratocarcinoma cell line.]. 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:2183156
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:43+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}