Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_provenance.
- NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_assertion wasGeneratedBy ECO_0000218 NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_provenance.
- NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_assertion wasDerivedFrom uniprot-20150221 NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_provenance.
- NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_assertion SIO_000772 12406339 NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_provenance.
- NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_assertion evidence source_evidence_curated NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_provenance.
- NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_assertion description "[A novel missense mutation affecting the human hairless thyroid receptor interacting domain 2 causes congenital atrichia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_provenance.