Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_provenance.
- befree-2016 importedOn "2016-02-19" NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_provenance.
- NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_assertion wasGeneratedBy ECO_0000203 NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_provenance.
- NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_assertion wasDerivedFrom befree-2016 NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_provenance.
- NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_assertion SIO_000772 15001591 NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_provenance.
- NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_assertion evidence source_evidence_literature NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_provenance.
- NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_assertion description "[Clinical features in the remaining 11 cases with no demonstrable KAL1 or FGFR1 mutations included right renal aplasia in one female, cleft palate in one male, cleft palate and perceptive deafness in one male, and dental agenesis and perceptive deafness in one male, in addition to a variable extent of HH and olfactory dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434304.RAZtnTxXAzMpwAzP59hf5NtNriI3yuX3Poj95I0qavt7g130_provenance.