Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_provenance.
- NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_assertion description "[Mutations in myotubularin, amphiphysin 2 (BIN1), and dynamin 2 lead to different forms of centronuclear myopathy, while mutations in myotubularin-related proteins cause Charcot-Marie-Tooth neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_provenance.
- NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_assertion evidence source_evidence_literature NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_provenance.
- NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_assertion SIO_000772 22496665 NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_provenance.
- NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_assertion wasDerivedFrom befree-20150227 NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_provenance.
- NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_assertion wasGeneratedBy ECO_0000203 NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP237742.RAXd4qdVk6rGU4GPQDKfzb60ClADknWYVwTkyuEGLGNP4130_provenance.