Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_provenance.
- NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_assertion description "[In 1994, the field of bone biology was significantly advanced by the discovery that activating mutations in the fibroblast growth factor receptor 3 (FGFR3) receptor tyrosine kinase (TK) account for the common genetic form of dwarfism in humans, achondroplasia (ACH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_provenance.
- NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_assertion evidence source_evidence_literature NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_provenance.
- NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_assertion SIO_000772 22045636 NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_provenance.
- NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_assertion wasDerivedFrom befree-20150227 NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_provenance.
- NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_assertion wasGeneratedBy ECO_0000203 NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP400917.RAffgpyT3RO5HVeD9QlrEjLxnTXlYium8TRcznTZE2-_k130_provenance.