Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP465022.RAnh1Adoz1wddNzEM4O1g55lip03UDAQRLSP0ez_SYnOA130_assertion> ?p ?o ?g. }
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- NP465022.RAnh1Adoz1wddNzEM4O1g55lip03UDAQRLSP0ez_SYnOA130_assertion type Assertion NP465022.RAnh1Adoz1wddNzEM4O1g55lip03UDAQRLSP0ez_SYnOA130_head.
- NP465022.RAnh1Adoz1wddNzEM4O1g55lip03UDAQRLSP0ez_SYnOA130_assertion description "[Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465022.RAnh1Adoz1wddNzEM4O1g55lip03UDAQRLSP0ez_SYnOA130_provenance.
- NP465022.RAnh1Adoz1wddNzEM4O1g55lip03UDAQRLSP0ez_SYnOA130_assertion evidence source_evidence_literature NP465022.RAnh1Adoz1wddNzEM4O1g55lip03UDAQRLSP0ez_SYnOA130_provenance.
- NP465022.RAnh1Adoz1wddNzEM4O1g55lip03UDAQRLSP0ez_SYnOA130_assertion SIO_000772 19855393 NP465022.RAnh1Adoz1wddNzEM4O1g55lip03UDAQRLSP0ez_SYnOA130_provenance.
- NP465022.RAnh1Adoz1wddNzEM4O1g55lip03UDAQRLSP0ez_SYnOA130_assertion wasDerivedFrom befree-20150227 NP465022.RAnh1Adoz1wddNzEM4O1g55lip03UDAQRLSP0ez_SYnOA130_provenance.
- NP465022.RAnh1Adoz1wddNzEM4O1g55lip03UDAQRLSP0ez_SYnOA130_assertion wasGeneratedBy ECO_0000203 NP465022.RAnh1Adoz1wddNzEM4O1g55lip03UDAQRLSP0ez_SYnOA130_provenance.