Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_provenance.
- NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_assertion description "[Hypochondroplasia and Acanthosis nigricans: a new syndrome due to the p.Lys650Thr mutation in the fibroblast growth factor receptor 3 gene?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_provenance.
- NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_assertion evidence source_evidence_literature NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_provenance.
- NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_assertion SIO_000772 18583390 NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_provenance.
- NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_assertion wasDerivedFrom befree-2016 NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_provenance.
- NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_assertion wasGeneratedBy ECO_0000203 NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_provenance.
- befree-2016 importedOn "2016-02-19" NP678959.RAnC7biBYXCgCwAcR3u4BQIu8bOVs3wv4yNCNR7OTJwWc130_provenance.