@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1388816.RAIkgYF-M6Hwybw6DLWIOYcKkpR69wU6w4amfGX_-yMXo130_head { this: np:hasAssertion dgn-np:NP1388816.RAIkgYF-M6Hwybw6DLWIOYcKkpR69wU6w4amfGX_-yMXo130_assertion; np:hasProvenance dgn-np:NP1388816.RAIkgYF-M6Hwybw6DLWIOYcKkpR69wU6w4amfGX_-yMXo130_provenance; np:hasPublicationInfo dgn-np:NP1388816.RAIkgYF-M6Hwybw6DLWIOYcKkpR69wU6w4amfGX_-yMXo130_publicationInfo; a np:Nanopublication . dgn-np:NP1388816.RAIkgYF-M6Hwybw6DLWIOYcKkpR69wU6w4amfGX_-yMXo130_assertion a np:Assertion . dgn-np:NP1388816.RAIkgYF-M6Hwybw6DLWIOYcKkpR69wU6w4amfGX_-yMXo130_provenance a np:Provenance . dgn-np:NP1388816.RAIkgYF-M6Hwybw6DLWIOYcKkpR69wU6w4amfGX_-yMXo130_publicationInfo a np:PublicationInfo . } dgn-np:NP1388816.RAIkgYF-M6Hwybw6DLWIOYcKkpR69wU6w4amfGX_-yMXo130_assertion { miriam-gene:5251 a ncit:C16612 . lld:C3540852 a ncit:C7057 . dgn-gda:DGNabb7fd36e4bd4b4841cb1e07a5dcf2d9 sio:SIO_000628 miriam-gene:5251, lld:C3540852; a sio:SIO_001121 . } dgn-np:NP1388816.RAIkgYF-M6Hwybw6DLWIOYcKkpR69wU6w4amfGX_-yMXo130_provenance { dgn-np:NP1388816.RAIkgYF-M6Hwybw6DLWIOYcKkpR69wU6w4amfGX_-yMXo130_assertion dcterms:description "[Two mouse mutations gyro (Gy) and hypophosphatemia (Hyp) are mouse models for X-linked hypophosphatemic rickets and have been shown to be deleted for the 5' and 3' end of the mouse homolog of PHEX (phosphate regulating gene with homologies to endopeptidases on the X chromosome; formerly called PEX), respectively.]. 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:9467015; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1388816.RAIkgYF-M6Hwybw6DLWIOYcKkpR69wU6w4amfGX_-yMXo130_publicationInfo { this: dcterms:created "2016-05-13T12:52:15+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }