Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_provenance.
- NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_assertion description "[The main features of McCune-Albright are fibrous dysplasia of bone (FD), caf�-au-lait macules and precocious puberty; the disease is caused by activating mutations in the Guanine Nucleotide-binding protein, Alpha-stimulating activity polypeptide (GNAS) gene which are always somatic.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_provenance.
- NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_assertion evidence source_evidence_literature NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_provenance.
- NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_assertion SIO_000772 24012779 NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_provenance.
- NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_assertion wasDerivedFrom befree-20150227 NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_provenance.
- NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_assertion wasGeneratedBy ECO_0000203 NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP429744.RALm6koc6LZRpwOAQGVVLclx-uHOdrxioGfe8wTQPWNhs130_provenance.