Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_provenance.
- NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_assertion description "[Here, we report on germline mutations of PHOX2B in both a familial case of NB and a patient with the HSCR-NB association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_provenance.
- NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_assertion evidence source_evidence_literature NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_provenance.
- NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_assertion SIO_000772 15024693 NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_provenance.
- NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_assertion wasDerivedFrom befree-20140225 NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_provenance.
- NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_assertion wasGeneratedBy ECO_0000203 NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_provenance.