@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP491925.RAiTJzSnJiOpO3EQ46qgfpDiRLP2J5qfe3ojxUDESvKqc
> .
@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:NP491925.RAiTJzSnJiOpO3EQ46qgfpDiRLP2J5qfe3ojxUDESvKqc130_head
{
this:
np:hasAssertion
dgn-np:NP491925.RAiTJzSnJiOpO3EQ46qgfpDiRLP2J5qfe3ojxUDESvKqc130_assertion
;
np:hasProvenance
dgn-np:NP491925.RAiTJzSnJiOpO3EQ46qgfpDiRLP2J5qfe3ojxUDESvKqc130_provenance
;
np:hasPublicationInfo
dgn-np:NP491925.RAiTJzSnJiOpO3EQ46qgfpDiRLP2J5qfe3ojxUDESvKqc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491925.RAiTJzSnJiOpO3EQ46qgfpDiRLP2J5qfe3ojxUDESvKqc130_assertion
a
np:Assertion
.
dgn-np:NP491925.RAiTJzSnJiOpO3EQ46qgfpDiRLP2J5qfe3ojxUDESvKqc130_provenance
a
np:Provenance
.
dgn-np:NP491925.RAiTJzSnJiOpO3EQ46qgfpDiRLP2J5qfe3ojxUDESvKqc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491925.RAiTJzSnJiOpO3EQ46qgfpDiRLP2J5qfe3ojxUDESvKqc130_assertion
{
miriam-gene:10181
a
ncit:C16612
.
lld:C0004509
a
ncit:C7057
.
dgn-gda:DGNb63abca7aad4483990a1aecc5a2d9576
sio:SIO_000628
miriam-gene:10181
,
lld:C0004509
;
a
sio:SIO_001121
.
}
dgn-np:NP491925.RAiTJzSnJiOpO3EQ46qgfpDiRLP2J5qfe3ojxUDESvKqc130_provenance
{
dgn-np:NP491925.RAiTJzSnJiOpO3EQ46qgfpDiRLP2J5qfe3ojxUDESvKqc130_assertion
dcterms:description
"[Mice carrying a missense mutation (R263P) in the second RNA recognition motif (RRM) of RBM5 exhibited spermatid differentiation arrest, germ cell sloughing and apoptosis, which ultimately led to azoospermia (no sperm in the ejaculate) and male sterility.]. 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:23935508
;
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:NP491925.RAiTJzSnJiOpO3EQ46qgfpDiRLP2J5qfe3ojxUDESvKqc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}