Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP487339.RAxB6dZnKzx5wrJnxuJw4vr0UdBu-dsXlXoMFpL2nn2sc130_assertion> ?p ?o ?g. }
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- NP487339.RAxB6dZnKzx5wrJnxuJw4vr0UdBu-dsXlXoMFpL2nn2sc130_assertion type Assertion NP487339.RAxB6dZnKzx5wrJnxuJw4vr0UdBu-dsXlXoMFpL2nn2sc130_head.
- NP487339.RAxB6dZnKzx5wrJnxuJw4vr0UdBu-dsXlXoMFpL2nn2sc130_assertion wasGeneratedBy ECO_0000203 NP487339.RAxB6dZnKzx5wrJnxuJw4vr0UdBu-dsXlXoMFpL2nn2sc130_provenance.
- NP487339.RAxB6dZnKzx5wrJnxuJw4vr0UdBu-dsXlXoMFpL2nn2sc130_assertion wasDerivedFrom befree-2016 NP487339.RAxB6dZnKzx5wrJnxuJw4vr0UdBu-dsXlXoMFpL2nn2sc130_provenance.
- NP487339.RAxB6dZnKzx5wrJnxuJw4vr0UdBu-dsXlXoMFpL2nn2sc130_assertion SIO_000772 15792865 NP487339.RAxB6dZnKzx5wrJnxuJw4vr0UdBu-dsXlXoMFpL2nn2sc130_provenance.
- NP487339.RAxB6dZnKzx5wrJnxuJw4vr0UdBu-dsXlXoMFpL2nn2sc130_assertion evidence source_evidence_literature NP487339.RAxB6dZnKzx5wrJnxuJw4vr0UdBu-dsXlXoMFpL2nn2sc130_provenance.
- NP487339.RAxB6dZnKzx5wrJnxuJw4vr0UdBu-dsXlXoMFpL2nn2sc130_assertion description "[An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP487339.RAxB6dZnKzx5wrJnxuJw4vr0UdBu-dsXlXoMFpL2nn2sc130_provenance.