Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP185562.RAdtWJFYzhPoyjwwVeryn6dSvkESPJsMFMWb4e1IIM44k130_assertion> ?p ?o ?g. }
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- NP185562.RAdtWJFYzhPoyjwwVeryn6dSvkESPJsMFMWb4e1IIM44k130_assertion type Assertion NP185562.RAdtWJFYzhPoyjwwVeryn6dSvkESPJsMFMWb4e1IIM44k130_head.
- NP185562.RAdtWJFYzhPoyjwwVeryn6dSvkESPJsMFMWb4e1IIM44k130_assertion description "[deficiency results in congenital disorders of glycosylation type Ig ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185562.RAdtWJFYzhPoyjwwVeryn6dSvkESPJsMFMWb4e1IIM44k130_provenance.
- NP185562.RAdtWJFYzhPoyjwwVeryn6dSvkESPJsMFMWb4e1IIM44k130_assertion evidence source_evidence_literature NP185562.RAdtWJFYzhPoyjwwVeryn6dSvkESPJsMFMWb4e1IIM44k130_provenance.
- NP185562.RAdtWJFYzhPoyjwwVeryn6dSvkESPJsMFMWb4e1IIM44k130_assertion SIO_000772 11983712 NP185562.RAdtWJFYzhPoyjwwVeryn6dSvkESPJsMFMWb4e1IIM44k130_provenance.
- NP185562.RAdtWJFYzhPoyjwwVeryn6dSvkESPJsMFMWb4e1IIM44k130_assertion wasDerivedFrom lhgdn-20090331 NP185562.RAdtWJFYzhPoyjwwVeryn6dSvkESPJsMFMWb4e1IIM44k130_provenance.
- NP185562.RAdtWJFYzhPoyjwwVeryn6dSvkESPJsMFMWb4e1IIM44k130_assertion wasGeneratedBy ECO_0000203 NP185562.RAdtWJFYzhPoyjwwVeryn6dSvkESPJsMFMWb4e1IIM44k130_provenance.