Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_assertion> ?p ?o ?g. }
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- NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_assertion type Assertion NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_head.
- NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_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." NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_provenance.
- NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_assertion evidence source_evidence_literature NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_provenance.
- NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_assertion SIO_000772 19054061 NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_provenance.
- NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_assertion wasDerivedFrom befree-20140225 NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_provenance.
- NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_assertion wasGeneratedBy ECO_0000203 NP320183.RAc381gBI0M9JTNxyBWyKomh8OjkrEUozTSfox4W0W7kQ130_provenance.