Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_assertion> ?p ?o ?g. }
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- NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_assertion type Assertion NP3714.RAr1oFGhNHJAXW6tra0rhlv6ELBM1NETHGcEQH6-B4efc130_head.
- 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.