Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_assertion> ?p ?o ?g. }
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- NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_assertion type Assertion NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_head.
- NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_assertion description "[In humans, mutations of RET or RET ligands are associated with the congenital abnormality Hirschsprung disease (HSCR) in which nerves and ganglia of the hind gut are absent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_provenance.
- NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_assertion evidence source_evidence_literature NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_provenance.
- NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_assertion SIO_000772 11409869 NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_provenance.
- NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_assertion wasDerivedFrom befree-2016 NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_provenance.
- NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_assertion wasGeneratedBy ECO_0000203 NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_provenance.