@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP841744.RAHltcXqhzH7-DAPX1pA9nnwYI19VafkLcJlI7W5wS06s
> .
@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:NP841744.RAHltcXqhzH7-DAPX1pA9nnwYI19VafkLcJlI7W5wS06s130_head
{
this:
np:hasAssertion
dgn-np:NP841744.RAHltcXqhzH7-DAPX1pA9nnwYI19VafkLcJlI7W5wS06s130_assertion
;
np:hasProvenance
dgn-np:NP841744.RAHltcXqhzH7-DAPX1pA9nnwYI19VafkLcJlI7W5wS06s130_provenance
;
np:hasPublicationInfo
dgn-np:NP841744.RAHltcXqhzH7-DAPX1pA9nnwYI19VafkLcJlI7W5wS06s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP841744.RAHltcXqhzH7-DAPX1pA9nnwYI19VafkLcJlI7W5wS06s130_assertion
a
np:Assertion
.
dgn-np:NP841744.RAHltcXqhzH7-DAPX1pA9nnwYI19VafkLcJlI7W5wS06s130_provenance
a
np:Provenance
.
dgn-np:NP841744.RAHltcXqhzH7-DAPX1pA9nnwYI19VafkLcJlI7W5wS06s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP841744.RAHltcXqhzH7-DAPX1pA9nnwYI19VafkLcJlI7W5wS06s130_assertion
{
miriam-gene:1553
a
ncit:C16612
.
lld:C0024591
a
ncit:C7057
.
dgn-gda:DGNfc5e16986cd2db104e41591e5cf4a18f
sio:SIO_000628
miriam-gene:1553
,
lld:C0024591
;
a
sio:SIO_001121
.
}
dgn-np:NP841744.RAHltcXqhzH7-DAPX1pA9nnwYI19VafkLcJlI7W5wS06s130_provenance
{
dgn-np:NP841744.RAHltcXqhzH7-DAPX1pA9nnwYI19VafkLcJlI7W5wS06s130_assertion
dcterms:description
"[However, segregation analysis with markers for D19S75, D19S28, D19S47, CYP2A, BCL3, and APOC2 shows that the crossovers in the first family involve the entire haplotype defined by these markers flanking RYR1 and, furthermore, reveals multiple crossovers between these haplotypes and MHS in the second family.]. 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:1598899
;
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:NP841744.RAHltcXqhzH7-DAPX1pA9nnwYI19VafkLcJlI7W5wS06s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:34+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" .
}