Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_provenance.
- NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_assertion description "[Clearly, low IGF1 levels are evidence of persistent severe GHD in subjects with genetic GHD or panhypopituitarism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_provenance.
- NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_assertion evidence source_evidence_literature NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_provenance.
- NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_assertion SIO_000772 18805914 NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_provenance.
- NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_assertion wasDerivedFrom befree-20150227 NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_provenance.
- NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_assertion wasGeneratedBy ECO_0000203 NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP482321.RAGuB6e_v4FfR2ddAwqZGbn52WOnxoHmXxBz1CBlxfPeA130_provenance.