Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_provenance.
- NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_assertion description "[Mutations in the p63 gene have been identified in five human disorders characterized by varying degrees of limb anomalies, ectodermal dysplasia, and facial clefts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_provenance.
- NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_assertion evidence source_evidence_literature NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_provenance.
- NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_assertion SIO_000772 16190990 NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_provenance.
- NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_assertion wasDerivedFrom befree-2016 NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_provenance.
- NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_assertion wasGeneratedBy ECO_0000203 NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_provenance.
- befree-2016 importedOn "2016-02-19" NP515500.RAUUolQhuo51gA2whO2txdZLoXljaUvyI5xA6ASrLrcqk130_provenance.