Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_provenance.
- NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_assertion description "[Dynamin 2 (DNM2)-related dominant centronuclear myopathy is usually a mild disorder, but more severe variants have been associated with mutations affecting the pleckstrin homology (PH) domain of the protein, mainly implicated in different forms of Charcot-Marie-Tooth Disease (CMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_provenance.
- NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_assertion evidence source_evidence_literature NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_provenance.
- NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_assertion SIO_000772 19932620 NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_provenance.
- NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_assertion wasDerivedFrom befree-20150227 NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_provenance.
- NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_assertion wasGeneratedBy ECO_0000203 NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_provenance.