@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP315358.RAAFTmjZjIugEdbJXDtwMrWvcALF41jCZiZGUnEm-pQkk
> .
@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:NP315358.RAAFTmjZjIugEdbJXDtwMrWvcALF41jCZiZGUnEm-pQkk130_head
{
this:
np:hasAssertion
dgn-np:NP315358.RAAFTmjZjIugEdbJXDtwMrWvcALF41jCZiZGUnEm-pQkk130_assertion
;
np:hasProvenance
dgn-np:NP315358.RAAFTmjZjIugEdbJXDtwMrWvcALF41jCZiZGUnEm-pQkk130_provenance
;
np:hasPublicationInfo
dgn-np:NP315358.RAAFTmjZjIugEdbJXDtwMrWvcALF41jCZiZGUnEm-pQkk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP315358.RAAFTmjZjIugEdbJXDtwMrWvcALF41jCZiZGUnEm-pQkk130_assertion
a
np:Assertion
.
dgn-np:NP315358.RAAFTmjZjIugEdbJXDtwMrWvcALF41jCZiZGUnEm-pQkk130_provenance
a
np:Provenance
.
dgn-np:NP315358.RAAFTmjZjIugEdbJXDtwMrWvcALF41jCZiZGUnEm-pQkk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP315358.RAAFTmjZjIugEdbJXDtwMrWvcALF41jCZiZGUnEm-pQkk130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGNee2c6b182fc1fc91b4c23e7c9818d9a1
sio:SIO_000628
miriam-gene:4292
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP315358.RAAFTmjZjIugEdbJXDtwMrWvcALF41jCZiZGUnEm-pQkk130_provenance
{
dgn-np:NP315358.RAAFTmjZjIugEdbJXDtwMrWvcALF41jCZiZGUnEm-pQkk130_assertion
dcterms:description
"[Mean numbers of MLH1 foci per cell, frequencies of cells presenting an MLH1 focus in the XY pair and percentages of cells affected by abnormal synaptic patterns (gaps and splits) are reported for each of the infertile patients and control men.]. 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:15890739
;
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:NP315358.RAAFTmjZjIugEdbJXDtwMrWvcALF41jCZiZGUnEm-pQkk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:00+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" .
}