Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_provenance.
- NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_assertion description "[The LGMD2C linked to chromosome 13q and related to a 35 KDa dystrophin-associated glycoprotein deficiency, is very similar to Duchenne muscular dystrophy with an autosomal recessive inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_provenance.
- NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_assertion evidence source_evidence_literature NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_provenance.
- NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_assertion SIO_000772 9027861 NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_provenance.
- NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_assertion wasDerivedFrom befree-20140225 NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_provenance.
- NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_assertion wasGeneratedBy ECO_0000203 NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP430005.RAEqHi1K87-gA9AWipmvKFwHQoPo1WQg9ixztwy0PCqWk130_provenance.