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- source_evidence_literature type ECO_0000212 NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_provenance.
- NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_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." NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_provenance.
- NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_assertion evidence source_evidence_literature NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_provenance.
- NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_assertion SIO_000772 19054061 NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_provenance.
- NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_assertion wasDerivedFrom befree-20150227 NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_provenance.
- NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_assertion wasGeneratedBy ECO_0000203 NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568176.RAMTz7ThivINYJxnyqOsNh0Qm6VCenUimmySk6BPXdbO8130_provenance.