Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP400914.RAWJVQVeudZqTuuX0Lq9JBsNfz_7w3wQdvIIvsLXlfIeo130_provenance.