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- source_evidence_literature type ECO_0000212 NP1057096.RAt4yJwy6dfdPsyKxqj8oMsieW6DVijFI_TS72ndXi9Lk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1057096.RAt4yJwy6dfdPsyKxqj8oMsieW6DVijFI_TS72ndXi9Lk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1057096.RAt4yJwy6dfdPsyKxqj8oMsieW6DVijFI_TS72ndXi9Lk130_provenance.
- NP1057096.RAt4yJwy6dfdPsyKxqj8oMsieW6DVijFI_TS72ndXi9Lk130_assertion description "[Constitutional mutations in RTEL1 cause severe dyskeratosis congenita.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1057096.RAt4yJwy6dfdPsyKxqj8oMsieW6DVijFI_TS72ndXi9Lk130_provenance.
- NP1057096.RAt4yJwy6dfdPsyKxqj8oMsieW6DVijFI_TS72ndXi9Lk130_assertion evidence source_evidence_literature NP1057096.RAt4yJwy6dfdPsyKxqj8oMsieW6DVijFI_TS72ndXi9Lk130_provenance.
- NP1057096.RAt4yJwy6dfdPsyKxqj8oMsieW6DVijFI_TS72ndXi9Lk130_assertion SIO_000772 23453664 NP1057096.RAt4yJwy6dfdPsyKxqj8oMsieW6DVijFI_TS72ndXi9Lk130_provenance.
- NP1057096.RAt4yJwy6dfdPsyKxqj8oMsieW6DVijFI_TS72ndXi9Lk130_assertion wasDerivedFrom befree-2016 NP1057096.RAt4yJwy6dfdPsyKxqj8oMsieW6DVijFI_TS72ndXi9Lk130_provenance.
- NP1057096.RAt4yJwy6dfdPsyKxqj8oMsieW6DVijFI_TS72ndXi9Lk130_assertion wasGeneratedBy ECO_0000203 NP1057096.RAt4yJwy6dfdPsyKxqj8oMsieW6DVijFI_TS72ndXi9Lk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1057096.RAt4yJwy6dfdPsyKxqj8oMsieW6DVijFI_TS72ndXi9Lk130_provenance.