Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_provenance.
- NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_assertion description "[This family represents a new syndrome (Mohr-Tranebjaerg syndrome, MTS) and provides significant new information about a new X linked recessive sydromic type of deafness which was previously thought to be isolated deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_provenance.
- NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_assertion evidence source_evidence_literature NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_provenance.
- NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_assertion SIO_000772 7643352 NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_provenance.
- NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_assertion wasDerivedFrom befree-20150227 NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_provenance.
- NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_assertion wasGeneratedBy ECO_0000203 NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_provenance.
- befree-20150227 importedOn "2015-02-27" NP353123.RAgv6WFS_-jeZ_x6HrdxricalZdEwTSFKWU3sa4RbDqns130_provenance.