Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_provenance.
- NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_assertion description "[Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_provenance.
- NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_assertion evidence source_evidence_curated NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_provenance.
- NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_assertion SIO_000772 16912710 NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_provenance.
- NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_assertion wasDerivedFrom uniprot-20130724 NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_provenance.
- NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_assertion wasGeneratedBy ECO_0000218 NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_provenance.