@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP496737.RAQAdDXFuyVYtWsohoZ0zIebPRkNlHAgnsqYzRSh4bnaw
> .
@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:NP496737.RAQAdDXFuyVYtWsohoZ0zIebPRkNlHAgnsqYzRSh4bnaw130_head
{
this:
np:hasAssertion
dgn-np:NP496737.RAQAdDXFuyVYtWsohoZ0zIebPRkNlHAgnsqYzRSh4bnaw130_assertion
;
np:hasProvenance
dgn-np:NP496737.RAQAdDXFuyVYtWsohoZ0zIebPRkNlHAgnsqYzRSh4bnaw130_provenance
;
np:hasPublicationInfo
dgn-np:NP496737.RAQAdDXFuyVYtWsohoZ0zIebPRkNlHAgnsqYzRSh4bnaw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP496737.RAQAdDXFuyVYtWsohoZ0zIebPRkNlHAgnsqYzRSh4bnaw130_assertion
a
np:Assertion
.
dgn-np:NP496737.RAQAdDXFuyVYtWsohoZ0zIebPRkNlHAgnsqYzRSh4bnaw130_provenance
a
np:Provenance
.
dgn-np:NP496737.RAQAdDXFuyVYtWsohoZ0zIebPRkNlHAgnsqYzRSh4bnaw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP496737.RAQAdDXFuyVYtWsohoZ0zIebPRkNlHAgnsqYzRSh4bnaw130_assertion
{
miriam-gene:6046
a
ncit:C16612
.
lld:C0021364
a
ncit:C7057
.
dgn-gda:DGN02b4221aa83e4292f25647b29655ed5d
sio:SIO_000628
miriam-gene:6046
,
lld:C0021364
;
a
sio:SIO_001121
.
}
dgn-np:NP496737.RAQAdDXFuyVYtWsohoZ0zIebPRkNlHAgnsqYzRSh4bnaw130_provenance
{
dgn-np:NP496737.RAQAdDXFuyVYtWsohoZ0zIebPRkNlHAgnsqYzRSh4bnaw130_assertion
dcterms:description
"[While Sertoli cell number and germ cell carrying capacity of the Sertoli cells in compromised in FSH mutants, both somatic and germ cell lineages are affected in the LH mutants resulting in complete male infertility.]. 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:16123236
;
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:NP496737.RAQAdDXFuyVYtWsohoZ0zIebPRkNlHAgnsqYzRSh4bnaw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:56+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" .
}