Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.
- NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_assertion description "[In humans, we identified recessive loss-of-function DYX1C1 mutations in 12 individuals with PCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.
- NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_assertion evidence source_evidence_literature NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.
- NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_assertion SIO_000772 23872636 NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.
- NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_assertion wasDerivedFrom befree-20150227 NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.
- NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_assertion wasGeneratedBy ECO_0000203 NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.