Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_provenance.
- NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_assertion description "[The founder member of this gene family, MTM1, is mutated in X-linked myotubular myopathy, a severe congenital disorder that affects skeletal muscle, and codes for myotubularin, a specific phosphatidylinositol 3-phosphate [PI(3)P] phosphatase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_provenance.
- NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_assertion evidence source_evidence_literature NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_provenance.
- NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_assertion SIO_000772 12217958 NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_provenance.
- NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_assertion wasDerivedFrom befree-2016 NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_provenance.
- NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_assertion wasGeneratedBy ECO_0000203 NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_provenance.
- befree-2016 importedOn "2016-02-19" NP367278.RAVgEJ4k4cgFxjOFgGOfncxU8_QyrN1QPNVjWcIaU7z2g130_provenance.