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- source_evidence_literature type ECO_0000212 NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_provenance.
- NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_assertion description "[Results of the rc mouse study, 3D structure predictions, homology with Myelin Protein Zero and EVA1, comprehensive database analyses of polymorphisms and mutations within the human MPZL3 gene and its cell, tissue expression and immunostaining pattern indicate that homozygous or compound heterozygous mutations of MPZL3 might be involved in immune-mediated human hereditary disorders with hair loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_provenance.
- NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_assertion evidence source_evidence_literature NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_provenance.
- NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_assertion SIO_000772 19054061 NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_provenance.
- NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_assertion wasDerivedFrom befree-20140225 NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_provenance.
- NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_assertion wasGeneratedBy ECO_0000203 NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP583238.RA3H8Qk04SX3rw1PqmBn5PJ-yLxHNy2mds5E6D3DJL1YA130_provenance.