Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_provenance.
- NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_assertion description "[Merosin (laminin-2 and -4; alpha 2-beta 1/beta 2-gamma 1) is the predominant laminin variant in skeletal muscle basement membranes; genetic defects affecting its structure or expression are the causes of some types of congenital muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_provenance.
- NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_assertion evidence source_evidence_literature NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_provenance.
- NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_assertion SIO_000772 8830776 NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_provenance.
- NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_assertion wasDerivedFrom befree-20140225 NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_provenance.
- NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_assertion wasGeneratedBy ECO_0000203 NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_provenance.