@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP160858.RA4fbPj0J7-B9t19S3W57WCP6eMub14IKzDCyRpTVk2Es
> .
@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:NP160858.RA4fbPj0J7-B9t19S3W57WCP6eMub14IKzDCyRpTVk2Es130_head
{
this:
np:hasAssertion
dgn-np:NP160858.RA4fbPj0J7-B9t19S3W57WCP6eMub14IKzDCyRpTVk2Es130_assertion
;
np:hasProvenance
dgn-np:NP160858.RA4fbPj0J7-B9t19S3W57WCP6eMub14IKzDCyRpTVk2Es130_provenance
;
np:hasPublicationInfo
dgn-np:NP160858.RA4fbPj0J7-B9t19S3W57WCP6eMub14IKzDCyRpTVk2Es130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP160858.RA4fbPj0J7-B9t19S3W57WCP6eMub14IKzDCyRpTVk2Es130_assertion
a
np:Assertion
.
dgn-np:NP160858.RA4fbPj0J7-B9t19S3W57WCP6eMub14IKzDCyRpTVk2Es130_provenance
a
np:Provenance
.
dgn-np:NP160858.RA4fbPj0J7-B9t19S3W57WCP6eMub14IKzDCyRpTVk2Es130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP160858.RA4fbPj0J7-B9t19S3W57WCP6eMub14IKzDCyRpTVk2Es130_assertion
{
miriam-gene:2261
a
ncit:C16612
.
lld:C0699885
a
ncit:C7057
.
dgn-gda:DGN057be7abfd390a4b07295ce208cde1f1
sio:SIO_000628
miriam-gene:2261
,
lld:C0699885
;
a
sio:SIO_001121
.
}
dgn-np:NP160858.RA4fbPj0J7-B9t19S3W57WCP6eMub14IKzDCyRpTVk2Es130_provenance
{
dgn-np:NP160858.RA4fbPj0J7-B9t19S3W57WCP6eMub14IKzDCyRpTVk2Es130_assertion
dcterms:description
"[Massively parallel sequencing of sperm DNA showed that levels of the FGFR3 mutation increase with paternal age and that the mutation spectrum at the Lys650 codon is similar to that observed in bladder cancer.]. 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:19855393
;
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:NP160858.RA4fbPj0J7-B9t19S3W57WCP6eMub14IKzDCyRpTVk2Es130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}