Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_provenance.
- NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_assertion description "[MYH9-related disorders may be associated with deafness and cataract; hence, Alport syndrome becomes important in the differential diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_provenance.
- NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_assertion evidence source_evidence_literature NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_provenance.
- NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_assertion SIO_000772 19726116 NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_provenance.
- NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_assertion wasDerivedFrom befree-20140225 NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_provenance.
- NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_assertion wasGeneratedBy ECO_0000203 NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP302761.RAEagNRkjiC3dZrcFelbue8Rpo1xEYCUNPam1CozUY8tM130_provenance.