Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_assertion> ?p ?o ?g. }
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- NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_assertion type Assertion NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_head.
- 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.