Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_assertion> ?p ?o ?g. }
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- NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_assertion type Assertion NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_head.
- NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_assertion description "[Achondroplasia (ACH), the most common form of human dwarfism is caused by a mutation in the Fibroblast Growth Factor Receptor 3 (FGFR3) gene, resulting in constitutive activation of the receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_provenance.
- NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_assertion evidence source_evidence_literature NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_provenance.
- NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_assertion SIO_000772 20673820 NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_provenance.
- NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_assertion wasDerivedFrom befree-20150227 NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_provenance.
- NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_assertion wasGeneratedBy ECO_0000203 NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_provenance.