Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_provenance.
- NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_assertion wasGeneratedBy ECO_0000203 NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_provenance.
- NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_assertion wasDerivedFrom befree-20150227 NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_provenance.
- NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_assertion SIO_000772 7508181 NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_provenance.
- NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_assertion evidence source_evidence_literature NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_provenance.
- NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_assertion description "[Recent studies in our laboratory established genetic linkage to the type II keratin gene locus on chromosome 12q in one family with EH and identified a single amino acid mutation in keratin 1 that is responsible for the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974109.RA7V5jM0ggGjF7-_i3M53tXnJuU3IzdANMAuiOthWtRRY130_provenance.