@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP822214.RAgt2k800moCL1D3sSKmxpSMJxC1Yh3utCuVSYQY04EYM
> .
@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:NP822214.RAgt2k800moCL1D3sSKmxpSMJxC1Yh3utCuVSYQY04EYM130_head
{
this:
np:hasAssertion
dgn-np:NP822214.RAgt2k800moCL1D3sSKmxpSMJxC1Yh3utCuVSYQY04EYM130_assertion
;
np:hasProvenance
dgn-np:NP822214.RAgt2k800moCL1D3sSKmxpSMJxC1Yh3utCuVSYQY04EYM130_provenance
;
np:hasPublicationInfo
dgn-np:NP822214.RAgt2k800moCL1D3sSKmxpSMJxC1Yh3utCuVSYQY04EYM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP822214.RAgt2k800moCL1D3sSKmxpSMJxC1Yh3utCuVSYQY04EYM130_assertion
a
np:Assertion
.
dgn-np:NP822214.RAgt2k800moCL1D3sSKmxpSMJxC1Yh3utCuVSYQY04EYM130_provenance
a
np:Provenance
.
dgn-np:NP822214.RAgt2k800moCL1D3sSKmxpSMJxC1Yh3utCuVSYQY04EYM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP822214.RAgt2k800moCL1D3sSKmxpSMJxC1Yh3utCuVSYQY04EYM130_assertion
{
miriam-gene:4140
a
ncit:C16612
.
lld:C0031269
a
ncit:C7057
.
dgn-gda:DGNf8b58fcf7260a35361fbd55e7b6a5501
sio:SIO_000628
miriam-gene:4140
,
lld:C0031269
;
a
sio:SIO_001121
.
}
dgn-np:NP822214.RAgt2k800moCL1D3sSKmxpSMJxC1Yh3utCuVSYQY04EYM130_provenance
{
dgn-np:NP822214.RAgt2k800moCL1D3sSKmxpSMJxC1Yh3utCuVSYQY04EYM130_assertion
dcterms:description
"[Furthermore, a MARK1, MARK2, MARK3 and MARK4 mutation analysis and an MARK4 quantitative multiplex polymerase chain reaction analysis to identify exon deletions on another eight PJS families without identified LKB1 germline mutation did not identify mutations in the MARK genes.]. 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:17924967
;
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:NP822214.RAgt2k800moCL1D3sSKmxpSMJxC1Yh3utCuVSYQY04EYM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:23+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" .
}