Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_provenance.
- befree-2016 importedOn "2016-02-19" NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_provenance.
- NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_assertion wasGeneratedBy ECO_0000203 NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_provenance.
- NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_assertion wasDerivedFrom befree-2016 NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_provenance.
- NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_assertion SIO_000772 17224651 NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_provenance.
- NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_assertion evidence source_evidence_literature NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_provenance.
- NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_assertion description "[Heterozygous mutations in the transcription factor gene p63 are causative for several syndromes, with ectodermal dysplasia, orofacial clefting and limb malformations as the key characteristics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588964.RA5B5sFz-sNvzDXCW2oKqqvarxVL9Nm1NzD3dd__vVr9c130_provenance.