Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.
- NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_assertion description "[Mutations of the myelin protein zero (MPZ) gene have been associated with CMT1B, Dejerine-Sottas disease, and congenital hypomyelination, which are inherited demyelinating neuropathies characterized by different clinical severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.
- NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_assertion evidence source_evidence_literature NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.
- NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_assertion SIO_000772 9595994 NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.
- NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_assertion wasDerivedFrom befree-2016 NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.
- NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_assertion wasGeneratedBy ECO_0000203 NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.
- befree-2016 importedOn "2016-02-19" NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.