Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_provenance.