Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP429288.RAX7Sb3qWpCMyXr9l7acrMThjj3Q_Z3w6sQpsSqbc1aUw130_assertion> ?p ?o ?g. }
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- NP429288.RAX7Sb3qWpCMyXr9l7acrMThjj3Q_Z3w6sQpsSqbc1aUw130_assertion type Assertion NP429288.RAX7Sb3qWpCMyXr9l7acrMThjj3Q_Z3w6sQpsSqbc1aUw130_head.
- NP429288.RAX7Sb3qWpCMyXr9l7acrMThjj3Q_Z3w6sQpsSqbc1aUw130_assertion description "[The identification of additional VLGR1 mutations to test whether a phenotype/genotype correlation exists, akin to that shown for other Usher syndrome disease genes, is warranted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429288.RAX7Sb3qWpCMyXr9l7acrMThjj3Q_Z3w6sQpsSqbc1aUw130_provenance.
- NP429288.RAX7Sb3qWpCMyXr9l7acrMThjj3Q_Z3w6sQpsSqbc1aUw130_assertion evidence source_evidence_literature NP429288.RAX7Sb3qWpCMyXr9l7acrMThjj3Q_Z3w6sQpsSqbc1aUw130_provenance.
- NP429288.RAX7Sb3qWpCMyXr9l7acrMThjj3Q_Z3w6sQpsSqbc1aUw130_assertion SIO_000772 14740321 NP429288.RAX7Sb3qWpCMyXr9l7acrMThjj3Q_Z3w6sQpsSqbc1aUw130_provenance.
- NP429288.RAX7Sb3qWpCMyXr9l7acrMThjj3Q_Z3w6sQpsSqbc1aUw130_assertion wasDerivedFrom befree-2016 NP429288.RAX7Sb3qWpCMyXr9l7acrMThjj3Q_Z3w6sQpsSqbc1aUw130_provenance.
- NP429288.RAX7Sb3qWpCMyXr9l7acrMThjj3Q_Z3w6sQpsSqbc1aUw130_assertion wasGeneratedBy ECO_0000203 NP429288.RAX7Sb3qWpCMyXr9l7acrMThjj3Q_Z3w6sQpsSqbc1aUw130_provenance.