@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:NP977709.RAWoJbef1-uVpgPIpAyERpHeor7kF_x7T_TFSX_HXN1rk130_head { this: np:hasAssertion dgn-np:NP977709.RAWoJbef1-uVpgPIpAyERpHeor7kF_x7T_TFSX_HXN1rk130_assertion; np:hasProvenance dgn-np:NP977709.RAWoJbef1-uVpgPIpAyERpHeor7kF_x7T_TFSX_HXN1rk130_provenance; np:hasPublicationInfo dgn-np:NP977709.RAWoJbef1-uVpgPIpAyERpHeor7kF_x7T_TFSX_HXN1rk130_publicationInfo; a np:Nanopublication . dgn-np:NP977709.RAWoJbef1-uVpgPIpAyERpHeor7kF_x7T_TFSX_HXN1rk130_assertion a np:Assertion . dgn-np:NP977709.RAWoJbef1-uVpgPIpAyERpHeor7kF_x7T_TFSX_HXN1rk130_provenance a np:Provenance . dgn-np:NP977709.RAWoJbef1-uVpgPIpAyERpHeor7kF_x7T_TFSX_HXN1rk130_publicationInfo a np:PublicationInfo . } dgn-np:NP977709.RAWoJbef1-uVpgPIpAyERpHeor7kF_x7T_TFSX_HXN1rk130_assertion { miriam-gene:9355 a ncit:C16612 . lld:C0002871 a ncit:C7057 . dgn-gda:DGNd70986c84d1eb8ac0698acda59f39e74 sio:SIO_000628 miriam-gene:9355, lld:C0002871; a sio:SIO_001121 . } dgn-np:NP977709.RAWoJbef1-uVpgPIpAyERpHeor7kF_x7T_TFSX_HXN1rk130_provenance { dgn-np:NP977709.RAWoJbef1-uVpgPIpAyERpHeor7kF_x7T_TFSX_HXN1rk130_assertion dcterms:description "[In the mouse, Lhx2, which encodes a member of the LIM (Lin-11, Isl-1, and Mec-3) class of homeodomain proteins, was shown to be expressed during early development in the posterior pituitary, eye, and liver, and its expression persists in adulthood in the central nervous system Lhx2(-/-) mice display absence of posterior pituitary and intermediate lobes, malformation of the anterior lobe, anophthalmia, and they die from anemia.]. 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:22535646; 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:NP977709.RAWoJbef1-uVpgPIpAyERpHeor7kF_x7T_TFSX_HXN1rk130_publicationInfo { this: dcterms:created "2016-05-13T12:49:08+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" . }